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nsv6930866

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:462,033

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1072 SVs from 66 studies. See in: genome view    
    Submitted genomic75,216,232-75,678,264Question Mark
    Overlapping variant regions from other studies: 1072 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):75,610,012-76,072,044Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930866Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,216,23275,678,264
    nsv6930866RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,610,01276,072,044

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18597823duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18597823Submitted genomicNC_000012.12:g.752
    16232_75678264dup
    GRCh38 (hg38)NC_000012.12Chr1275,216,23275,678,264
    nssv18597823RemappedPerfectNC_000012.11:g.756
    10012_76072044dup
    GRCh37.p13First PassNC_000012.11Chr1275,610,01276,072,044

    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)
    nssv185978234e-061270660
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