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nsv6960104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:840

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 72 SVs from 14 studies. See in: genome view    
    Submitted genomic64,953,713-64,954,552Question Mark
    Overlapping variant regions from other studies: 72 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):65,420,431-65,421,270Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,953,71364,954,552
    nsv6960104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,420,43165,421,270

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18614592duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18614592Submitted genomicNC_000014.9:g.6495
    3713_64954552dup
    GRCh38 (hg38)NC_000014.9Chr1464,953,71364,954,552
    nssv18614592RemappedPerfectNC_000014.8:g.6542
    0431_65421270dup
    GRCh37.p13First PassNC_000014.8Chr1465,420,43165,421,270

    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)
    nssv186145928e-062258750
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