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nsv7028529

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,880

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 26 studies. See in: genome view    
    Submitted genomic36,256,702-36,266,581Question Mark
    Overlapping variant regions from other studies: 134 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):34,844,624-34,854,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028529Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2036,256,70236,266,581
    nsv7028529RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2034,844,62434,854,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431930deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431930Submitted genomicNC_000020.11:g.362
    56702_36266581del
    GRCh38 (hg38)NC_000020.11Chr2036,256,70236,266,581
    nssv18431930RemappedPerfectNC_000020.10:g.348
    44624_34854503del
    GRCh37.p13First PassNC_000020.10Chr2034,844,62434,854,503

    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)
    nssv184319306.7e-0519275506
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