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nsv6656954

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,131

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 217 SVs from 49 studies. See in: genome view    
    Submitted genomic96,013,541-96,034,671Question Mark
    Overlapping variant regions from other studies: 217 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):96,479,097-96,500,227Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6656954Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr196,013,54196,034,671
    nsv6656954RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr196,479,09796,500,227

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641850duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641850Submitted genomicNC_000001.11:g.960
    13541_96034671dup
    GRCh38 (hg38)NC_000001.11Chr196,013,54196,034,671
    nssv18641850RemappedPerfectNC_000001.10:g.964
    79097_96500227dup
    GRCh37.p13First PassNC_000001.10Chr196,479,09796,500,227

    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)
    nssv186418506.4e-0518274584
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