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nsv4421375

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:442,580

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3081 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):27,245,155-27,687,734Question Mark
    Overlapping variant regions from other studies: 3081 SVs from 76 studies. See in: genome view    
    Submitted genomic27,736,063-28,178,642Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4421375RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1927,245,15527,245,15527,681,75927,687,734
    nsv4421375Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1927,736,06327,736,06328,172,66728,178,642

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15726848copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15726848RemappedPerfectNC_000019.10:g.(27
    245155_27245155)_(
    27681759_27687734)
    del    		GRCh38.p12First PassNC_000019.10Chr1927,245,15527,245,15527,681,75927,687,734
    nssv15726848Submitted genomicNC_000019.9:g.(277
    36063_27736063)_(2
    8172667_28178642)d
    el    		GRCh37 (hg19)NC_000019.9Chr1927,736,06327,736,06328,172,66728,178,642

    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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