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nsv6855885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,806

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 26 studies. See in: genome view    
    Submitted genomic64,648,363-64,657,168Question Mark
    Overlapping variant regions from other studies: 124 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):65,560,920-65,569,725Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6855885Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr864,648,36364,657,168
    nsv6855885RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr865,560,92065,569,725

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18557980deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18557980Submitted genomicNC_000008.11:g.646
    48363_64657168del
    GRCh38 (hg38)NC_000008.11Chr864,648,36364,657,168
    nssv18557980RemappedPerfectNC_000008.10:g.655
    60920_65569725del
    GRCh37.p13First PassNC_000008.10Chr865,560,92065,569,725

    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)
    nssv185579804e-061276262
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