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nsv4415590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:326,049

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 729 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):71,582,829-71,908,877Question Mark
    Overlapping variant regions from other studies: 728 SVs from 71 studies. See in: genome view    
    Submitted genomic71,293,875-71,619,923Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4415590RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1171,582,82971,616,62271,904,51371,908,877
    nsv4415590Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1171,293,87571,327,66871,615,55971,619,923

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15708765copy number gainMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15708765RemappedPerfectNC_000011.10:g.(71
    582829_71616622)_(
    71904513_71908877)
    dup    		GRCh38.p12First PassNC_000011.10Chr1171,582,82971,616,62271,904,51371,908,877
    nssv15708765Submitted genomicNC_000011.9:g.(712
    93875_71327668)_(7
    1615559_71619923)d
    up    		GRCh37 (hg19)NC_000011.9Chr1171,293,87571,327,66871,615,55971,619,923

    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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