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nsv4404665

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:297,575

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3783 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):11,929,504-12,227,078Question Mark
    Overlapping variant regions from other studies: 3787 SVs from 104 studies. See in: genome view    
    Submitted genomic11,929,504-12,227,078Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4404665RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr911,929,50411,933,67412,177,66012,227,078
    nsv4404665Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr911,929,50411,933,67412,177,66012,227,078

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15743502copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15743502RemappedPerfectNC_000009.12:g.(11
    929504_11933674)_(
    12177660_12227078)
    del    		GRCh38.p12First PassNC_000009.12Chr911,929,50411,933,67412,177,66012,227,078
    nssv15743502Submitted genomicNC_000009.11:g.(11
    929504_11933674)_(
    12177660_12227078)
    del    		GRCh37 (hg19)NC_000009.11Chr911,929,50411,933,67412,177,66012,227,078

    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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