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nsv6720864

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,347

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 180 SVs from 36 studies. See in: genome view    
    Submitted genomic186,786,474-186,794,820Question Mark
    Overlapping variant regions from other studies: 180 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):186,504,263-186,512,609Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720864Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3186,786,474186,794,820
    nsv6720864RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3186,504,263186,512,609

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18673955duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18673955Submitted genomicNC_000003.12:g.186
    786474_186794820du
    p
    GRCh38 (hg38)NC_000003.12Chr3186,786,474186,794,820
    nssv18673955RemappedPerfectNC_000003.11:g.186
    504263_186512609du
    p
    GRCh37.p13First PassNC_000003.11Chr3186,504,263186,512,609

    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)
    nssv18673955<0.00175275672
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