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nsv6997359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:628,605

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1825 SVs from 98 studies. See in: genome view    
    Submitted genomic14,524,308-15,152,912Question Mark
    Overlapping variant regions from other studies: 1825 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):14,427,625-15,056,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1714,524,30815,152,912
    nsv6997359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1714,427,62515,056,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18405940deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18405940Submitted genomicNC_000017.11:g.145
    24308_15152912del
    GRCh38 (hg38)NC_000017.11Chr1714,524,30815,152,912
    nssv18405940RemappedPerfectNC_000017.10:g.144
    27625_15056229del
    GRCh37.p13First PassNC_000017.10Chr1714,427,62515,056,229

    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)
    nssv184059404e-061276234
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