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nsv7047135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:966,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3145 SVs from 94 studies. See in: genome view    
    Submitted genomic112,389,397-113,355,432Question Mark
    Overlapping variant regions from other studies: 3146 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):112,932,019-113,898,054Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047135Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,389,397113,355,432
    nsv7047135RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1112,932,019113,898,054

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18735916inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18735916Submitted genomicNC_000001.11:g.112
    389397_113355432in
    v
    GRCh38 (hg38)NC_000001.11Chr1112,389,397113,355,432
    nssv18735916RemappedPerfectNC_000001.10:g.112
    932019_113898054in
    v
    GRCh37.p13First PassNC_000001.10Chr1112,932,019113,898,054

    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)
    nssv187359164e-061276268
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