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nsv7070433

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,136,846

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6197 SVs from 130 studies. See in: genome view    
    Submitted genomic28,680,335-30,817,180Question Mark
    Overlapping variant regions from other studies: 6198 SVs from 130 studies. See in: genome view    
    Remapped(Score: Good):28,925,481-31,109,383Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070433Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1528,680,33530,817,180
    nsv7070433RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1528,925,48131,109,383

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755973inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755973Submitted genomicNC_000015.10:g.286
    80335_30817180inv
    GRCh38 (hg38)NC_000015.10Chr1528,680,33530,817,180
    nssv18755973RemappedGoodNC_000015.9:g.2892
    5481_31109383inv
    GRCh37.p13First PassNC_000015.9Chr1528,925,48131,109,383

    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)
    nssv18755973<0.00140267430
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