U.S. flag

An official website of the United States government

nsv6607668

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:479,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1746 SVs from 95 studies. See in: genome view    
    Submitted genomic100,428,001-100,907,900Question Mark
    Overlapping variant regions from other studies: 1746 SVs from 95 studies. See in: genome view    
    Remapped(Score: Good):100,025,624-100,505,520Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6607668Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,428,001100,907,900
    nsv6607668RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7100,025,624100,505,520

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18233531duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18233531Submitted genomicNC_000007.14:g.100
    428001_100907900du
    p
    GRCh38 (hg38)NC_000007.14Chr7100,428,001100,907,900
    nssv18233531RemappedGoodNC_000007.13:g.100
    025624_100505520du
    p
    GRCh37.p13First PassNC_000007.13Chr7100,025,624100,505,520

    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)
    nssv18233531<0.001238596
    Support Center