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nsv6857558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,149

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 219 SVs from 38 studies. See in: genome view    
    Submitted genomic67,431,446-67,469,594Question Mark
    Overlapping variant regions from other studies: 219 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):68,343,681-68,381,829Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr867,431,44667,469,594
    nsv6857558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr868,343,68168,381,829

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18555912deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18555912Submitted genomicNC_000008.11:g.674
    31446_67469594del
    GRCh38 (hg38)NC_000008.11Chr867,431,44667,469,594
    nssv18555912RemappedPerfectNC_000008.10:g.683
    43681_68381829del
    GRCh37.p13First PassNC_000008.10Chr868,343,68168,381,829

    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)
    nssv185559124e-061276264
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