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nsv7007182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,289

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 196 SVs from 38 studies. See in: genome view    
    Submitted genomic2,296,754-2,311,042Question Mark
    Overlapping variant regions from other studies: 196 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):2,296,753-2,311,041Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7007182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr192,296,7542,311,042
    nsv7007182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr192,296,7532,311,041

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18421769deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18421769Submitted genomicNC_000019.10:g.229
    6754_2311042del
    GRCh38 (hg38)NC_000019.10Chr192,296,7542,311,042
    nssv18421769RemappedPerfectNC_000019.9:g.2296
    753_2311041del
    GRCh37.p13First PassNC_000019.9Chr192,296,7532,311,041

    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)
    nssv184217697e-062276150
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