U.S. flag

An official website of the United States government

nsv6931692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,149

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 36 studies. See in: genome view    
    Submitted genomic75,298,820-75,336,968Question Mark
    Overlapping variant regions from other studies: 165 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):75,692,600-75,730,748Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931692Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,298,82075,336,968
    nsv6931692RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,692,60075,730,748

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18597828duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18597828Submitted genomicNC_000012.12:g.752
    98820_75336968dup
    GRCh38 (hg38)NC_000012.12Chr1275,298,82075,336,968
    nssv18597828RemappedPerfectNC_000012.11:g.756
    92600_75730748dup
    GRCh37.p13First PassNC_000012.11Chr1275,692,60075,730,748

    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)
    nssv185978281.8e-055274422
    Support Center