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nsv6752896

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 27 studies. See in: genome view    
    Submitted genomic71,397,201-71,399,400Question Mark
    Overlapping variant regions from other studies: 117 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):72,262,918-72,265,117Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6752896Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr471,397,20171,399,400
    nsv6752896RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr472,262,91872,265,117

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18695255duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18695255Submitted genomicNC_000004.12:g.713
    97201_71399400dup
    GRCh38 (hg38)NC_000004.12Chr471,397,20171,399,400
    nssv18695255RemappedPerfectNC_000004.11:g.722
    62918_72265117dup
    GRCh37.p13First PassNC_000004.11Chr472,262,91872,265,117

    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)
    nssv186952554.3e-0512270306
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