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nsv6645752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:716

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 30 studies. See in: genome view    
    Submitted genomic180,349,279-180,349,994Question Mark
    Overlapping variant regions from other studies: 174 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):180,318,414-180,319,129Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6645752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1180,349,279180,349,994
    nsv6645752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1180,318,414180,319,129

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364262deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364262Submitted genomicNC_000001.11:g.180
    349279_180349994de
    l
    GRCh38 (hg38)NC_000001.11Chr1180,349,279180,349,994
    nssv18364262RemappedPerfectNC_000001.10:g.180
    318414_180319129de
    l
    GRCh37.p13First PassNC_000001.10Chr1180,318,414180,319,129

    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)
    nssv18364262<0.00162268356
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