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nsv6887551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:224,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 779 SVs from 66 studies. See in: genome view    
    Submitted genomic43,244,701-43,469,100Question Mark
    Overlapping variant regions from other studies: 776 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):43,740,149-43,964,548Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6887551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1043,244,70143,469,100
    nsv6887551RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1043,740,14943,964,548

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581400duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581400Submitted genomicNC_000010.11:g.432
    44701_43469100dup
    GRCh38 (hg38)NC_000010.11Chr1043,244,70143,469,100
    nssv18581400RemappedPerfectNC_000010.10:g.437
    40149_43964548dup
    GRCh37.p13First PassNC_000010.10Chr1043,740,14943,964,548

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18581400<0.001138249296
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