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nsv6720505

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,622

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 35 studies. See in: genome view    
    Submitted genomic141,767,928-141,776,549Question Mark
    Overlapping variant regions from other studies: 143 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):141,486,770-141,495,391Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720505Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,767,928141,776,549
    nsv6720505RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,486,770141,495,391

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18473024deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18473024Submitted genomicNC_000003.12:g.141
    767928_141776549de
    l
    GRCh38 (hg38)NC_000003.12Chr3141,767,928141,776,549
    nssv18473024RemappedPerfectNC_000003.11:g.141
    486770_141495391de
    l
    GRCh37.p13First PassNC_000003.11Chr3141,486,770141,495,391

    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)
    nssv184730244e-061276252
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