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nsv6722497

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:778,033

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1803 SVs from 83 studies. See in: genome view    
    Submitted genomic161,334,993-162,113,025Question Mark
    Overlapping variant regions from other studies: 1803 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):161,052,781-161,830,813Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6722497Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3161,334,993162,113,025
    nsv6722497RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3161,052,781161,830,813

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18674285duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18674285Submitted genomicNC_000003.12:g.161
    334993_162113025du
    p
    GRCh38 (hg38)NC_000003.12Chr3161,334,993162,113,025
    nssv18674285RemappedPerfectNC_000003.11:g.161
    052781_161830813du
    p
    GRCh37.p13First PassNC_000003.11Chr3161,052,781161,830,813

    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)
    nssv186742854e-061273956
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