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nsv6643648

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,047

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Submitted genomic163,147,501-163,152,547Question Mark
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):163,117,291-163,122,337Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643648Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,147,501163,152,547
    nsv6643648RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,117,291163,122,337

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364473deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364473Submitted genomicNC_000001.11:g.163
    147501_163152547de
    l
    GRCh38 (hg38)NC_000001.11Chr1163,147,501163,152,547
    nssv18364473RemappedPerfectNC_000001.10:g.163
    117291_163122337de
    l
    GRCh37.p13First PassNC_000001.10Chr1163,117,291163,122,337

    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)
    nssv183644731.8e-055275536
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