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nsv7058136

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:90

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 21 studies. See in: genome view    
    Submitted genomic29,281,651-29,281,740Question Mark
    Overlapping variant regions from other studies: 120 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):29,434,584-29,434,673Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058136Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,281,65129,281,740
    nsv7058136RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,434,58429,434,673

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751767inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751767Submitted genomicNC_000012.12:g.292
    81651_29281740inv
    GRCh38 (hg38)NC_000012.12Chr1229,281,65129,281,740
    nssv18751767RemappedPerfectNC_000012.11:g.294
    34584_29434673inv
    GRCh37.p13First PassNC_000012.11Chr1229,434,58429,434,673

    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)
    nssv187517674e-061276268
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