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nsv6937670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:508

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Submitted genomic94,999,215-94,999,722Question Mark
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):95,392,991-95,393,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1294,999,21594,999,722
    nsv6937670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1295,392,99195,393,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600362duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600362Submitted genomicNC_000012.12:g.949
    99215_94999722dup
    GRCh38 (hg38)NC_000012.12Chr1294,999,21594,999,722
    nssv18600362RemappedPerfectNC_000012.11:g.953
    92991_95393498dup
    GRCh37.p13First PassNC_000012.11Chr1295,392,99195,393,498

    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)
    nssv18600362<0.001139237672
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