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nsv6857881

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,331

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
    Submitted genomic97,853,343-97,856,673Question Mark
    Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):98,865,571-98,868,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857881Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr897,853,34397,856,673
    nsv6857881RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr898,865,57198,868,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18561127deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18561127Submitted genomicNC_000008.11:g.978
    53343_97856673del
    GRCh38 (hg38)NC_000008.11Chr897,853,34397,856,673
    nssv18561127RemappedPerfectNC_000008.10:g.988
    65571_98868901del
    GRCh37.p13First PassNC_000008.10Chr898,865,57198,868,901

    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)
    nssv185611274e-061275426
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