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nsv7077659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 26 studies. See in: genome view    
    Submitted genomic31,319,700-31,321,392Question Mark
    Overlapping variant regions from other studies: 153 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):32,692,015-32,693,707Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2131,319,70031,321,392
    nsv7077659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2132,692,01532,693,707

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763122inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763122Submitted genomicNC_000021.9:g.3131
    9700_31321392inv
    GRCh38 (hg38)NC_000021.9Chr2131,319,70031,321,392
    nssv18763122RemappedPerfectNC_000021.8:g.3269
    2015_32693707inv
    GRCh37.p13First PassNC_000021.8Chr2132,692,01532,693,707

    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)
    nssv187631220.001274267470
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