U.S. flag

An official website of the United States government

nsv6697913

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:104

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 17 studies. See in: genome view    
    Submitted genomic134,400,738-134,400,841Question Mark
    Overlapping variant regions from other studies: 110 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):135,158,309-135,158,412Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6697913Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2134,400,738134,400,841
    nsv6697913RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2135,158,309135,158,412

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18649522duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18649522Submitted genomicNC_000002.12:g.134
    400738_134400841du
    p
    GRCh38 (hg38)NC_000002.12Chr2134,400,738134,400,841
    nssv18649522RemappedPerfectNC_000002.11:g.135
    158309_135158412du
    p
    GRCh37.p13First PassNC_000002.11Chr2135,158,309135,158,412

    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)
    nssv18649522<0.00155224796
    Support Center