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nsv6133206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,280,294

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 34286 SVs from 133 studies. See in: genome view    
    Remapped(Score: Good):74,426,102-84,706,395Question Mark
    Overlapping variant regions from other studies: 34282 SVs from 133 studies. See in: genome view    
    Submitted genomic74,460,000-84,740,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6133206RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1674,426,10284,706,395
    nsv6133206Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr1674,460,00084,740,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17681355copy number lossSAMN20524664SequencingPaired-end mapping739

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17681355RemappedGoodNC_000016.10:g.744
    26102_84706395del
    GRCh38.p12First PassNC_000016.10Chr1674,426,10284,706,395
    nssv17681355Submitted genomicNC_000016.9:g.7446
    0000_84740001del
    GRCh37 (hg19)NC_000016.9Chr1674,460,00084,740,001

    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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