U.S. flag

An official website of the United States government

nsv6712141

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:433,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1917 SVs from 85 studies. See in: genome view    
    Submitted genomic240,048,501-240,481,500Question Mark
    Overlapping variant regions from other studies: 1917 SVs from 85 studies. See in: genome view    
    Remapped(Score: Perfect):240,987,918-241,420,917Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6712141Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2240,048,501240,481,500
    nsv6712141RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2240,987,918241,420,917

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664328duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664328Submitted genomicNC_000002.12:g.240
    048501_240481500du
    p
    GRCh38 (hg38)NC_000002.12Chr2240,048,501240,481,500
    nssv18664328RemappedPerfectNC_000002.11:g.240
    987918_241420917du
    p
    GRCh37.p13First PassNC_000002.11Chr2240,987,918241,420,917

    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)
    nssv186643284e-061275260
    Support Center