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nsv6643846

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,955

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 19 studies. See in: genome view    
    Submitted genomic165,422,895-165,425,849Question Mark
    Overlapping variant regions from other studies: 119 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):165,392,132-165,395,086Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643846Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1165,422,895165,425,849
    nsv6643846RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1165,392,132165,395,086

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363198deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363198Submitted genomicNC_000001.11:g.165
    422895_165425849de
    l
    GRCh38 (hg38)NC_000001.11Chr1165,422,895165,425,849
    nssv18363198RemappedPerfectNC_000001.10:g.165
    392132_165395086de
    l
    GRCh37.p13First PassNC_000001.10Chr1165,392,132165,395,086

    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)
    nssv183631984e-061275940
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