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nsv4403535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113,920

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 373 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):129,380,821-129,494,740Question Mark
    Overlapping variant regions from other studies: 373 SVs from 62 studies. See in: genome view    
    Submitted genomic129,099,664-129,213,583Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4403535RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3129,380,821129,382,591129,489,366129,494,740
    nsv4403535Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3129,099,664129,101,434129,208,209129,213,583

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15732839copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15732839RemappedPerfectNC_000003.12:g.(12
    9380821_129382591)
    _(129489366_129494
    740)del    		GRCh38.p12First PassNC_000003.12Chr3129,380,821129,382,591129,489,366129,494,740
    nssv15732839Submitted genomicNC_000003.11:g.(12
    9099664_129101434)
    _(129208209_129213
    583)del    		GRCh37 (hg19)NC_000003.11Chr3129,099,664129,101,434129,208,209129,213,583

    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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