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nsv6134898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100,002

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3549 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):164,918,848-166,018,849Question Mark
    Overlapping variant regions from other studies: 3549 SVs from 97 studies. See in: genome view    
    Submitted genomic165,840,000-166,940,001Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6134898RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4164,918,848166,018,849
    nsv6134898Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4165,840,000166,940,001

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17683083copy number lossSAMN20524662SequencingPaired-end mapping1,603

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17683083RemappedPerfectNC_000004.12:g.164
    918848_166018849de
    l
    GRCh38.p12First PassNC_000004.12Chr4164,918,848166,018,849
    nssv17683083Submitted genomicNC_000004.11:g.165
    840000_166940001de
    l
    GRCh37 (hg19)NC_000004.11Chr4165,840,000166,940,001

    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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