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nsv6711625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,220

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 30 studies. See in: genome view    
    Submitted genomic121,460,926-121,462,145Question Mark
    Overlapping variant regions from other studies: 116 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):121,179,773-121,180,992Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3121,460,926121,462,145
    nsv6711625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3121,179,773121,180,992

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18670618duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18670618Submitted genomicNC_000003.12:g.121
    460926_121462145du
    p
    GRCh38 (hg38)NC_000003.12Chr3121,460,926121,462,145
    nssv18670618RemappedPerfectNC_000003.11:g.121
    179773_121180992du
    p
    GRCh37.p13First PassNC_000003.11Chr3121,179,773121,180,992

    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)
    nssv186706183.3e-059263660
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