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nsv4410377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 430 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):26,874,437-27,021,618Question Mark
    Overlapping variant regions from other studies: 429 SVs from 70 studies. See in: genome view    
    Submitted genomic26,842,216-26,989,397Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4410377RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr626,874,43726,892,11027,003,99527,021,618
    nsv4410377Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr626,842,21626,859,88926,971,77426,989,397

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15712085copy number gainMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15712085RemappedPerfectNC_000006.12:g.(26
    874437_26892110)_(
    27003995_27021618)
    dup    		GRCh38.p12First PassNC_000006.12Chr626,874,43726,892,11027,003,99527,021,618
    nssv15712085Submitted genomicNC_000006.11:g.(26
    842216_26859889)_(
    26971774_26989397)
    dup    		GRCh37 (hg19)NC_000006.11Chr626,842,21626,859,88926,971,77426,989,397

    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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