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nsv6994087

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,233

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 327 SVs from 62 studies. See in: genome view    
    Submitted genomic22,361,904-22,375,136Question Mark
    Overlapping variant regions from other studies: 327 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):22,373,225-22,386,457Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6994087Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1622,361,90422,375,136
    nsv6994087RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1622,373,22522,386,457

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398436deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398436Submitted genomicNC_000016.10:g.223
    61904_22375136del
    GRCh38 (hg38)NC_000016.10Chr1622,361,90422,375,136
    nssv18398436RemappedPerfectNC_000016.9:g.2237
    3225_22386457del
    GRCh37.p13First PassNC_000016.9Chr1622,373,22522,386,457

    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)
    nssv183984364e-061276260
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