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nsv4412141

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:487,607

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2430 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):66,238,608-66,726,214Question Mark
    Overlapping variant regions from other studies: 2430 SVs from 107 studies. See in: genome view    
    Submitted genomic66,948,501-67,436,107Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv4412141RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr666,238,60866,241,20466,709,81766,726,214
    nsv4412141Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr666,948,50166,951,09767,419,71067,436,107

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv15738576copy number lossMultipleMultiple

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv15738576RemappedPerfectNC_000006.12:g.(66
    238608_66241204)_(
    66709817_66726214)
    del    		GRCh38.p12First PassNC_000006.12Chr666,238,60866,241,20466,709,81766,726,214
    nssv15738576Submitted genomicNC_000006.11:g.(66
    948501_66951097)_(
    67419710_67436107)
    del    		GRCh37 (hg19)NC_000006.11Chr666,948,50166,951,09767,419,71067,436,107

    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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