U.S. flag

An official website of the United States government

nsv7045576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:475,419

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2864 SVs from 111 studies. See in: genome view    
    Submitted genomic180,805,627-181,281,045Question Mark
    Overlapping variant regions from other studies: 2865 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):180,232,627-180,708,046Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,805,627181,281,045
    nsv7045576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,232,627180,708,046

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775931inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775931Submitted genomicNC_000005.10:g.180
    805627_181281045in
    v
    GRCh38 (hg38)NC_000005.10Chr5180,805,627181,281,045
    nssv18775931RemappedPerfectNC_000005.9:g.1802
    32627_180708046inv
    GRCh37.p13First PassNC_000005.9Chr5180,232,627180,708,046

    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)
    nssv187759317e-062273174
    Support Center