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nsv6863570

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,115

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Submitted genomic111,631,744-111,639,858Question Mark
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):114,394,024-114,402,138Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6863570Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,631,744111,639,858
    nsv6863570RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,394,024114,402,138

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18562027deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18562027Submitted genomicNC_000009.12:g.111
    631744_111639858de
    l
    GRCh38 (hg38)NC_000009.12Chr9111,631,744111,639,858
    nssv18562027RemappedPerfectNC_000009.11:g.114
    394024_114402138de
    l
    GRCh37.p13First PassNC_000009.11Chr9114,394,024114,402,138

    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)
    nssv18562027<0.00136261216
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