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nsv6859395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,208

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 88 SVs from 24 studies. See in: genome view    
    Submitted genomic122,186,139-122,196,346Question Mark
    Overlapping variant regions from other studies: 88 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):124,948,418-124,958,625Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6859395Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,186,139122,196,346
    nsv6859395RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,948,418124,958,625

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18562116deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18562116Submitted genomicNC_000009.12:g.122
    186139_122196346de
    l
    GRCh38 (hg38)NC_000009.12Chr9122,186,139122,196,346
    nssv18562116RemappedPerfectNC_000009.11:g.124
    948418_124958625de
    l
    GRCh37.p13First PassNC_000009.11Chr9124,948,418124,958,625

    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)
    nssv185621164e-061276194
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