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nsv6807691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Submitted genomic108,937,900-108,938,396Question Mark
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):109,259,103-109,259,599Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6807691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6108,937,900108,938,396
    nsv6807691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,259,103109,259,599

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18517420deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18517420Submitted genomicNC_000006.12:g.108
    937900_108938396de
    l
    GRCh38 (hg38)NC_000006.12Chr6108,937,900108,938,396
    nssv18517420RemappedPerfectNC_000006.11:g.109
    259103_109259599de
    l
    GRCh37.p13First PassNC_000006.11Chr6109,259,103109,259,599

    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)
    nssv18517420<0.001177264984
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