U.S. flag

An official website of the United States government

nsv6810863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:291,047

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1059 SVs from 81 studies. See in: genome view    
    Submitted genomic17,248,220-17,539,266Question Mark
    Overlapping variant regions from other studies: 1059 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):17,287,844-17,578,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6810863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr717,248,22017,539,266
    nsv6810863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr717,287,84417,578,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723564duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723564Submitted genomicNC_000007.14:g.172
    48220_17539266dup
    GRCh38 (hg38)NC_000007.14Chr717,248,22017,539,266
    nssv18723564RemappedPerfectNC_000007.13:g.172
    87844_17578890dup
    GRCh37.p13First PassNC_000007.13Chr717,287,84417,578,890

    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)
    nssv187235644e-061274642
    Support Center