U.S. flag

An official website of the United States government

nsv6832921

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 37 studies. See in: genome view    
    Submitted genomic64,693,534-64,693,557Question Mark
    Overlapping variant regions from other studies: 139 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):64,153,912-64,153,935Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832921Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr764,693,53464,693,557
    nsv6832921RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr764,153,91264,153,935

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18543289deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18543289Submitted genomicNC_000007.14:g.646
    93534_64693557del
    GRCh38 (hg38)NC_000007.14Chr764,693,53464,693,557
    nssv18543289RemappedPerfectNC_000007.13:g.641
    53912_64153935del
    GRCh37.p13First PassNC_000007.13Chr764,153,91264,153,935

    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)
    nssv18543289<0.00191220500
    Support Center