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nsv6643557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,713

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 25 studies. See in: genome view    
    Submitted genomic163,201,729-163,209,441Question Mark
    Overlapping variant regions from other studies: 128 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):163,171,519-163,179,231Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,201,729163,209,441
    nsv6643557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,171,519163,179,231

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18589131duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18589131Submitted genomicNC_000001.11:g.163
    201729_163209441du
    p
    GRCh38 (hg38)NC_000001.11Chr1163,201,729163,209,441
    nssv18589131RemappedPerfectNC_000001.10:g.163
    171519_163179231du
    p
    GRCh37.p13First PassNC_000001.10Chr1163,171,519163,179,231

    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)
    nssv185891314e-061275970
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