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nsv6720575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,487

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 32 studies. See in: genome view    
    Submitted genomic141,770,582-141,773,068Question Mark
    Overlapping variant regions from other studies: 122 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):141,489,424-141,491,910Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,770,582141,773,068
    nsv6720575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,489,424141,491,910

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18473025deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18473025Submitted genomicNC_000003.12:g.141
    770582_141773068de
    l
    GRCh38 (hg38)NC_000003.12Chr3141,770,582141,773,068
    nssv18473025RemappedPerfectNC_000003.11:g.141
    489424_141491910de
    l
    GRCh37.p13First PassNC_000003.11Chr3141,489,424141,491,910

    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)
    nssv184730251.4e-054275230
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