nsv6956640

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,682

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 188 SVs from 39 studies. See in: genome view    
    Submitted genomic20,319,368-20,350,049Question Mark
    Overlapping variant regions from other studies: 188 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):20,787,527-20,818,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6956640Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,319,36820,350,049
    nsv6956640RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1420,787,52720,818,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18383858deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18383858Submitted genomicNC_000014.9:g.2031
    9368_20350049del
    GRCh38 (hg38)NC_000014.9Chr1420,319,36820,350,049
    nssv18383858RemappedPerfectNC_000014.8:g.2078
    7527_20818208del
    GRCh37.p13First PassNC_000014.8Chr1420,787,52720,818,208

    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)
    nssv183838584e-061275922
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