U.S. flag

An official website of the United States government

nsv7073207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,825

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 272 SVs from 58 studies. See in: genome view    
    Submitted genomic71,538,472-71,581,296Question Mark
    Overlapping variant regions from other studies: 272 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):71,249,518-71,292,342Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073207Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1171,538,47271,581,296
    nsv7073207RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1171,249,51871,292,342

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740623inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740623Submitted genomicNC_000011.10:g.715
    38472_71581296inv
    GRCh38 (hg38)NC_000011.10Chr1171,538,47271,581,296
    nssv18740623RemappedPerfectNC_000011.9:g.7124
    9518_71292342inv
    GRCh37.p13First PassNC_000011.9Chr1171,249,51871,292,342

    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)
    nssv187406233.2e-059274746
    Support Center