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nsv6956320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 397 SVs from 57 studies. See in: genome view    
    Submitted genomic69,828,901-69,875,900Question Mark
    Overlapping variant regions from other studies: 397 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):70,403,033-70,450,032Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6956320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1369,828,90169,875,900
    nsv6956320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1370,403,03370,450,032

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18380809deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18380809Submitted genomicNC_000013.11:g.698
    28901_69875900del
    GRCh38 (hg38)NC_000013.11Chr1369,828,90169,875,900
    nssv18380809RemappedPerfectNC_000013.10:g.704
    03033_70450032del
    GRCh37.p13First PassNC_000013.10Chr1370,403,03370,450,032

    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)
    nssv18380809<0.00167238304
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