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nsv7074580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,387,464

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15264 SVs from 108 studies. See in: genome view    
    Submitted genomic110,243,158-113,630,621Question Mark
    Overlapping variant regions from other studies: 15245 SVs from 108 studies. See in: genome view    
    Remapped(Score: Good):110,895,505-114,284,936Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13110,243,158113,630,621
    nsv7074580RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13110,895,505114,284,936

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752128inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752128Submitted genomicNC_000013.11:g.110
    243158_113630621in
    v
    GRCh38 (hg38)NC_000013.11Chr13110,243,158113,630,621
    nssv18752128RemappedGoodNC_000013.10:g.110
    895505_114284936in
    v
    GRCh37.p13First PassNC_000013.10Chr13110,895,505114,284,936

    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)
    nssv187521284e-061276268
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