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nsv6993828

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,056

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 195 SVs from 34 studies. See in: genome view    
    Submitted genomic32,399,553-32,432,608Question Mark
    Overlapping variant regions from other studies: 195 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):30,726,572-30,759,627Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993828Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1732,399,55332,432,608
    nsv6993828RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1730,726,57230,759,627

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625843duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625843Submitted genomicNC_000017.11:g.323
    99553_32432608dup
    GRCh38 (hg38)NC_000017.11Chr1732,399,55332,432,608
    nssv18625843RemappedPerfectNC_000017.10:g.307
    26572_30759627dup
    GRCh37.p13First PassNC_000017.10Chr1730,726,57230,759,627

    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)
    nssv186258436.8e-0519275242
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