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nsv6857598

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,828

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 15 studies. See in: genome view    
    Submitted genomic93,526,869-93,530,696Question Mark
    Overlapping variant regions from other studies: 138 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):94,539,097-94,542,924Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6857598Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr893,526,86993,530,696
    nsv6857598RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr894,539,09794,542,924

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18561745deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18561745Submitted genomicNC_000008.11:g.935
    26869_93530696del
    GRCh38 (hg38)NC_000008.11Chr893,526,86993,530,696
    nssv18561745RemappedPerfectNC_000008.10:g.945
    39097_94542924del
    GRCh37.p13First PassNC_000008.10Chr894,539,09794,542,924

    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)
    nssv18561745<0.00164275792
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