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nsv6131758

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108,780

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 391 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):29,089,062-29,197,841Question Mark
    Overlapping variant regions from other studies: 391 SVs from 47 studies. See in: genome view    
    Submitted genomic29,377,991-29,486,770Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6131758RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1029,089,06229,089,08129,197,82229,197,841
    nsv6131758Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1029,377,99129,378,01029,486,75129,486,770

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17680519inversionSAMN20524657SequencingPaired-end mapping656

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17680519RemappedPerfectNC_000010.11:g.(29
    089062_29089081)_(
    29197822_29197841)
    inv    		GRCh38.p12First PassNC_000010.11Chr1029,089,06229,089,08129,197,82229,197,841
    nssv17680519Submitted genomicNC_000010.10:g.(29
    377991_29378010)_(
    29486751_29486770)
    inv    		GRCh37 (hg19)NC_000010.10Chr1029,377,99129,378,01029,486,75129,486,770

    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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