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nsv6988215

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,354

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 308 SVs from 44 studies. See in: genome view    
    Submitted genomic16,932,347-16,954,700Question Mark
    Overlapping variant regions from other studies: 308 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):16,835,661-16,858,014Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6988215Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1716,932,34716,954,700
    nsv6988215RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1716,835,66116,858,014

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626960duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626960Submitted genomicNC_000017.11:g.169
    32347_16954700dup
    GRCh38 (hg38)NC_000017.11Chr1716,932,34716,954,700
    nssv18626960RemappedPerfectNC_000017.10:g.168
    35661_16858014dup
    GRCh37.p13First PassNC_000017.10Chr1716,835,66116,858,014

    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)
    nssv186269604e-061275364
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