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nsv6731260

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:307

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 44 studies. See in: genome view    
    Submitted genomic154,378,958-154,379,264Question Mark
    Overlapping variant regions from other studies: 142 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):154,096,747-154,097,053Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6731260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,378,958154,379,264
    nsv6731260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,096,747154,097,053

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18474643deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18474643Submitted genomicNC_000003.12:g.154
    378958_154379264de
    l
    GRCh38 (hg38)NC_000003.12Chr3154,378,958154,379,264
    nssv18474643RemappedPerfectNC_000003.11:g.154
    096747_154097053de
    l
    GRCh37.p13First PassNC_000003.11Chr3154,096,747154,097,053

    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)
    nssv184746430.941258772274960
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