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nsv7040651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62,146

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 284 SVs from 64 studies. See in: genome view    
    Submitted genomic29,335,328-29,397,473Question Mark
    Overlapping variant regions from other studies: 284 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):29,303,105-29,365,250Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr629,335,32829,397,473
    nsv7040651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,303,10529,365,250

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778550inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778550Submitted genomicNC_000006.12:g.293
    35328_29397473inv
    GRCh38 (hg38)NC_000006.12Chr629,335,32829,397,473
    nssv18778550RemappedPerfectNC_000006.11:g.293
    03105_29365250inv
    GRCh37.p13First PassNC_000006.11Chr629,303,10529,365,250

    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)
    nssv187785504e-061276268
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