nsv7054428

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,177

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 984 SVs from 97 studies. See in: genome view    
    Submitted genomic31,437,767-31,492,943Question Mark
    Overlapping variant regions from other studies: 984 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):31,405,544-31,460,720Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054428Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,437,76731,492,943
    nsv7054428RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,405,54431,460,720

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778583inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778583Submitted genomicNC_000006.12:g.314
    37767_31492943inv
    GRCh38 (hg38)NC_000006.12Chr631,437,76731,492,943
    nssv18778583RemappedPerfectNC_000006.11:g.314
    05544_31460720inv
    GRCh37.p13First PassNC_000006.11Chr631,405,54431,460,720

    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)
    nssv187785834e-061276268
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