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nsv6988061

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 25 studies. See in: genome view    
    Submitted genomic39,475,129-39,477,957Question Mark
    Overlapping variant regions from other studies: 137 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):37,631,382-37,634,210Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6988061Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,475,12939,477,957
    nsv6988061RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,631,38237,634,210

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18409241deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18409241Submitted genomicNC_000017.11:g.394
    75129_39477957del
    GRCh38 (hg38)NC_000017.11Chr1739,475,12939,477,957
    nssv18409241RemappedPerfectNC_000017.10:g.376
    31382_37634210del
    GRCh37.p13First PassNC_000017.10Chr1737,631,38237,634,210

    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)
    nssv184092411.4e-054273720
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