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nsv6643555

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,320

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
    Submitted genomic163,138,947-163,142,266Question Mark
    Overlapping variant regions from other studies: 126 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):163,108,737-163,112,056Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643555Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,138,947163,142,266
    nsv6643555RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,108,737163,112,056

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364472deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364472Submitted genomicNC_000001.11:g.163
    138947_163142266de
    l
    GRCh38 (hg38)NC_000001.11Chr1163,138,947163,142,266
    nssv18364472RemappedPerfectNC_000001.10:g.163
    108737_163112056de
    l
    GRCh37.p13First PassNC_000001.10Chr1163,108,737163,112,056

    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)
    nssv183644720.001293275060
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