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nsv6717698

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105,468

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 389 SVs from 51 studies. See in: genome view    
    Submitted genomic113,477,918-113,583,385Question Mark
    Overlapping variant regions from other studies: 389 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):113,196,765-113,302,232Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6717698Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3113,477,918113,583,385
    nsv6717698RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3113,196,765113,302,232

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18668042duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18668042Submitted genomicNC_000003.12:g.113
    477918_113583385du
    p
    GRCh38 (hg38)NC_000003.12Chr3113,477,918113,583,385
    nssv18668042RemappedPerfectNC_000003.11:g.113
    196765_113302232du
    p
    GRCh37.p13First PassNC_000003.11Chr3113,196,765113,302,232

    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)
    nssv186680421.1e-053271804
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