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nsv6917254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 16 studies. See in: genome view    
    Submitted genomic88,509,271-88,509,323Question Mark
    Overlapping variant regions from other studies: 95 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):88,242,439-88,242,491Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6917254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1188,509,27188,509,323
    nsv6917254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1188,242,43988,242,491

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353613deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353613Submitted genomicNC_000011.10:g.885
    09271_88509323del
    GRCh38 (hg38)NC_000011.10Chr1188,509,27188,509,323
    nssv18353613RemappedPerfectNC_000011.9:g.8824
    2439_88242491del
    GRCh37.p13First PassNC_000011.9Chr1188,242,43988,242,491

    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)
    nssv183536133.4e-059255864
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