U.S. flag

An official website of the United States government

nsv6772634

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 325 SVs from 32 studies. See in: genome view    
    Submitted genomic16,173,101-16,230,200Question Mark
    Overlapping variant regions from other studies: 325 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):16,173,210-16,230,309Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6772634Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr516,173,10116,230,200
    nsv6772634RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr516,173,21016,230,309

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18697860duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18697860Submitted genomicNC_000005.10:g.161
    73101_16230200dup
    GRCh38 (hg38)NC_000005.10Chr516,173,10116,230,200
    nssv18697860RemappedPerfectNC_000005.9:g.1617
    3210_16230309dup
    GRCh37.p13First PassNC_000005.9Chr516,173,21016,230,309

    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)
    nssv186978604e-061272658
    Support Center