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nsv6898565

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 37 studies. See in: genome view    
    Submitted genomic5,231,901-5,240,300Question Mark
    Overlapping variant regions from other studies: 162 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):5,253,131-5,261,530Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6898565Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr115,231,9015,240,300
    nsv6898565RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,253,1315,261,530

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351458deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351458Submitted genomicNC_000011.10:g.523
    1901_5240300del
    GRCh38 (hg38)NC_000011.10Chr115,231,9015,240,300
    nssv18351458RemappedPerfectNC_000011.9:g.5253
    131_5261530del
    GRCh37.p13First PassNC_000011.9Chr115,253,1315,261,530

    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)
    nssv18351458<0.00131255358
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