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nsv6990797

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 21 studies. See in: genome view    
    Submitted genomic58,776,601-58,780,100Question Mark
    Overlapping variant regions from other studies: 123 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):56,853,962-56,857,461Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990797Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,776,60158,780,100
    nsv6990797RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,853,96256,857,461

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413147deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413147Submitted genomicNC_000017.11:g.587
    76601_58780100del
    GRCh38 (hg38)NC_000017.11Chr1758,776,60158,780,100
    nssv18413147RemappedPerfectNC_000017.10:g.568
    53962_56857461del
    GRCh37.p13First PassNC_000017.10Chr1756,853,96256,857,461

    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)
    nssv184131472.1e-056274932
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