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nsv6990015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 278 SVs from 38 studies. See in: genome view    
    Submitted genomic19,421,401-19,431,000Question Mark
    Overlapping variant regions from other studies: 278 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):19,324,714-19,334,313Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1719,421,40119,431,000
    nsv6990015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1719,324,71419,334,313

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407533deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407533Submitted genomicNC_000017.11:g.194
    21401_19431000del
    GRCh38 (hg38)NC_000017.11Chr1719,421,40119,431,000
    nssv18407533RemappedPerfectNC_000017.10:g.193
    24714_19334313del
    GRCh37.p13First PassNC_000017.10Chr1719,324,71419,334,313

    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)
    nssv18407533<0.001116253760
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