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nsv4430416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,581

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 727 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):23,355,603-23,472,183Question Mark
    Overlapping variant regions from other studies: 728 SVs from 28 studies. See in: genome view    
    Submitted genomic25,501,750-25,618,330Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4430416RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY23,355,60323,385,69023,472,10223,472,183
    nsv4430416Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000024.9ChrY25,501,75025,531,83725,618,24925,618,330

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15713545copy number gainMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15713545RemappedPerfectNC_000024.10:g.(23
    355603_23385690)_(
    23472102_23472183)
    dup    		GRCh38.p12First PassNC_000024.10ChrY23,355,60323,385,69023,472,10223,472,183
    nssv15713545Submitted genomicNC_000024.9:g.(255
    01750_25531837)_(2
    5618249_25618330)d
    up    		GRCh37 (hg19)NC_000024.9ChrY25,501,75025,531,83725,618,24925,618,330

    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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