U.S. flag

An official website of the United States government

nsv7041088

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:208,185

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 519 SVs from 57 studies. See in: genome view    
    Submitted genomic73,616,710-73,824,894Question Mark
    Overlapping variant regions from other studies: 519 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):73,665,861-73,874,045Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041088Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr373,616,71073,824,894
    nsv7041088RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr373,665,86173,874,045

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772074inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772074Submitted genomicNC_000003.12:g.736
    16710_73824894inv
    GRCh38 (hg38)NC_000003.12Chr373,616,71073,824,894
    nssv18772074RemappedPerfectNC_000003.11:g.736
    65861_73874045inv
    GRCh37.p13First PassNC_000003.11Chr373,665,86173,874,045

    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)
    nssv187720741.1e-053274950
    Support Center