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nsv6984163

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:317,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1698 SVs from 89 studies. See in: genome view    
    Submitted genomic85,142,364-85,459,522Question Mark
    Overlapping variant regions from other studies: 1698 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):85,175,970-85,493,128Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984163Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1685,142,36485,459,522
    nsv6984163RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1685,175,97085,493,128

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407052deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407052Submitted genomicNC_000016.10:g.851
    42364_85459522del
    GRCh38 (hg38)NC_000016.10Chr1685,142,36485,459,522
    nssv18407052RemappedPerfectNC_000016.9:g.8517
    5970_85493128del
    GRCh37.p13First PassNC_000016.9Chr1685,175,97085,493,128

    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)
    nssv184070524e-061276220
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