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nsv6996308

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,132

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 18 studies. See in: genome view    
    Submitted genomic58,872,622-58,874,753Question Mark
    Overlapping variant regions from other studies: 118 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):56,949,983-56,952,114Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6996308Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,872,62258,874,753
    nsv6996308RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,949,98356,952,114

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413160deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413160Submitted genomicNC_000017.11:g.588
    72622_58874753del
    GRCh38 (hg38)NC_000017.11Chr1758,872,62258,874,753
    nssv18413160RemappedPerfectNC_000017.10:g.569
    49983_56952114del
    GRCh37.p13First PassNC_000017.10Chr1756,949,98356,952,114

    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)
    nssv184131604e-061271050
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