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nsv6995992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 17 studies. See in: genome view    
    Submitted genomic32,830,677-32,830,753Question Mark
    Overlapping variant regions from other studies: 87 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):31,157,695-31,157,771Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1732,830,67732,830,753
    nsv6995992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1731,157,69531,157,771

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626107duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626107Submitted genomicNC_000017.11:g.328
    30677_32830753dup
    GRCh38 (hg38)NC_000017.11Chr1732,830,67732,830,753
    nssv18626107RemappedPerfectNC_000017.10:g.311
    57695_31157771dup
    GRCh37.p13First PassNC_000017.10Chr1731,157,69531,157,771

    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)
    nssv186261079e-062222860
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