U.S. flag

An official website of the United States government

nsv6329396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:424,445

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1357 SVs from 88 studies. See in: genome view    
    Submitted genomic212,832,753-213,257,197Question Mark
    Overlapping variant regions from other studies: 1363 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):213,006,095-213,430,540Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6329396Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1212,832,753213,257,197
    nsv6329396RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1213,006,095213,430,540

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18200544duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18200544Submitted genomicNC_000001.11:g.212
    832753_213257197du
    p
    GRCh38 (hg38)NC_000001.11Chr1212,832,753213,257,197
    nssv18200544RemappedPerfectNC_000001.10:g.213
    006095_213430540du
    p
    GRCh37.p13First PassNC_000001.10Chr1213,006,095213,430,540

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18200544<0.001139304
    Support Center