The 1000 genomes snp and short indel all get submitted to dbSNP and longer structural variants get submitted to the DGVa

The pilot project snps have all been accessioned by dbSNP and are available in dbSNP 132. The pilot project structural variants are being processed by the DGVa

No main project variants calls have yet been processed by either archive.

Please note that archiving these variants is a long process so there can be a delay of a few months between new variants being discovered and then being loaded into one of the archives. The absence of a 1000 genomes variant from an archive probably means it has not yet been accessioned by that archive. The 1000 genomes project is also discovering many novel snps which were not part of previous studies like HapMap.