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nsv6450354

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:226

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 214 SVs from 54 studies. See in: genome view    
    Submitted genomic39,096,070-39,096,295Question Mark
    Overlapping variant regions from other studies: 312 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):39,096,067-39,096,292Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6450354Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr939,096,07039,096,295
    nsv6450354RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr939,096,06739,096,292

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18193180deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18193180Submitted genomicNC_000009.12:g.390
    96070_39096295del
    GRCh38 (hg38)NC_000009.12Chr939,096,07039,096,295
    nssv18193180RemappedPerfectNC_000009.11:g.390
    96067_39096292del
    GRCh37.p13First PassNC_000009.11Chr939,096,06739,096,292

    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)
    nssv18193180<0.0011821710
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