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nsv6990323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,384

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Submitted genomic66,860,351-66,862,734Question Mark
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):64,856,469-64,858,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1766,860,35166,862,734
    nsv6990323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1764,856,46964,858,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18413597deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18413597Submitted genomicNC_000017.11:g.668
    60351_66862734del
    GRCh38 (hg38)NC_000017.11Chr1766,860,35166,862,734
    nssv18413597RemappedPerfectNC_000017.10:g.648
    56469_64858852del
    GRCh37.p13First PassNC_000017.10Chr1764,856,46964,858,852

    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)
    nssv18413597<0.00133275400
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