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nsv6736382

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,623

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 770 SVs from 79 studies. See in: genome view    
    Submitted genomic195,685,867-195,694,489Question Mark
    Overlapping variant regions from other studies: 774 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):195,412,738-195,421,360Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6736382Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3195,685,867195,694,489
    nsv6736382RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3195,412,738195,421,360

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18479336deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18479336Submitted genomicNC_000003.12:g.195
    685867_195694489de
    l
    GRCh38 (hg38)NC_000003.12Chr3195,685,867195,694,489
    nssv18479336RemappedPerfectNC_000003.11:g.195
    412738_195421360de
    l
    GRCh37.p13First PassNC_000003.11Chr3195,412,738195,421,360

    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)
    nssv18479336<0.00161263982
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