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nsv7043244

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,807

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 19 studies. See in: genome view    
    Submitted genomic154,346,788-154,355,594Question Mark
    Overlapping variant regions from other studies: 104 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):154,064,577-154,073,383Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043244Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,346,788154,355,594
    nsv7043244RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,064,577154,073,383

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770300inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770300Submitted genomicNC_000003.12:g.154
    346788_154355594in
    v
    GRCh38 (hg38)NC_000003.12Chr3154,346,788154,355,594
    nssv18770300RemappedPerfectNC_000003.11:g.154
    064577_154073383in
    v
    GRCh37.p13First PassNC_000003.11Chr3154,064,577154,073,383

    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)
    nssv187703004e-061276266
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