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nsv6992860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,795

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 22 studies. See in: genome view    
    Submitted genomic39,093,846-39,095,640Question Mark
    Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):37,250,099-37,251,893Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,093,84639,095,640
    nsv6992860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,250,09937,251,893

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628699duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628699Submitted genomicNC_000017.11:g.390
    93846_39095640dup
    GRCh38 (hg38)NC_000017.11Chr1739,093,84639,095,640
    nssv18628699RemappedPerfectNC_000017.10:g.372
    50099_37251893dup
    GRCh37.p13First PassNC_000017.10Chr1737,250,09937,251,893

    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)
    nssv186286999.1e-056259506
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