U.S. flag

An official website of the United States government

nsv7073198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,365,022

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5120 SVs from 89 studies. See in: genome view    
    Submitted genomic109,606,328-111,971,349Question Mark
    Overlapping variant regions from other studies: 5120 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):111,366,086-113,731,107Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10109,606,328111,971,349
    nsv7073198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10111,366,086113,731,107

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749219inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749219Submitted genomicNC_000010.11:g.109
    606328_111971349in
    v
    GRCh38 (hg38)NC_000010.11Chr10109,606,328111,971,349
    nssv18749219RemappedPerfectNC_000010.10:g.111
    366086_113731107in
    v
    GRCh37.p13First PassNC_000010.10Chr10111,366,086113,731,107

    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)
    nssv187492194e-061276268
    Support Center