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nsv6136065

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,580,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6382 SVs from 118 studies. See in: genome view    
    Remapped(Score: Perfect):55,907,441-58,487,442Question Mark
    Overlapping variant regions from other studies: 6382 SVs from 118 studies. See in: genome view    
    Submitted genomic56,820,000-59,400,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6136065RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr855,907,44158,487,442
    nsv6136065Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr856,820,00059,400,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17683189copy number lossSAMN20524662SequencingPaired-end mapping1,603

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17683189RemappedPerfectNC_000008.11:g.559
    07441_58487442del
    GRCh38.p12First PassNC_000008.11Chr855,907,44158,487,442
    nssv17683189Submitted genomicNC_000008.10:g.568
    20000_59400001del
    GRCh37 (hg19)NC_000008.10Chr856,820,00059,400,001

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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