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nsv7074837

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,490,570

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8784 SVs from 113 studies. See in: genome view    
    Submitted genomic98,618,777-101,109,346Question Mark
    Overlapping variant regions from other studies: 8786 SVs from 113 studies. See in: genome view    
    Remapped(Score: Good):99,162,006-101,649,551Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074837Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1598,618,777101,109,346
    nsv7074837RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1599,162,006101,649,551

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756753inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756753Submitted genomicNC_000015.10:g.986
    18777_101109346inv
    GRCh38 (hg38)NC_000015.10Chr1598,618,777101,109,346
    nssv18756753RemappedGoodNC_000015.9:g.9916
    2006_101649551inv
    GRCh37.p13First PassNC_000015.9Chr1599,162,006101,649,551

    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)
    nssv187567531.4e-054270814
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