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nsv6657471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,315

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
    Submitted genomic94,259,496-94,269,810Question Mark
    Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):94,725,052-94,735,366Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6657471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr194,259,49694,269,810
    nsv6657471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,725,05294,735,366

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18428956deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18428956Submitted genomicNC_000001.11:g.942
    59496_94269810del
    GRCh38 (hg38)NC_000001.11Chr194,259,49694,269,810
    nssv18428956RemappedPerfectNC_000001.10:g.947
    25052_94735366del
    GRCh37.p13First PassNC_000001.10Chr194,725,05294,735,366

    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)
    nssv18428956<0.0011275824
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