U.S. flag

An official website of the United States government

nsv7040757

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:587,823

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1720 SVs from 71 studies. See in: genome view    
    Submitted genomic119,358,756-119,946,578Question Mark
    Overlapping variant regions from other studies: 1719 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):118,492,719-119,080,541Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040757Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX119,358,756119,946,578
    nsv7040757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX118,492,719119,080,541

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764642inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764642Submitted genomicNC_000023.11:g.119
    358756_119946578in
    v
    GRCh38 (hg38)NC_000023.11ChrX119,358,756119,946,578
    nssv18764642RemappedPerfectNC_000023.10:g.118
    492719_119080541in
    v
    GRCh37.p13First PassNC_000023.10ChrX118,492,719119,080,541

    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)
    nssv187646425e-061200000
    Support Center