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nsv7053416

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 16 studies. See in: genome view    
    Submitted genomic236,730,941-236,731,025Question Mark
    Overlapping variant regions from other studies: 147 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):236,894,241-236,894,325Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053416Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1236,730,941236,731,025
    nsv7053416RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1236,894,241236,894,325

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759345inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759345Submitted genomicNC_000001.11:g.236
    730941_236731025in
    v
    GRCh38 (hg38)NC_000001.11Chr1236,730,941236,731,025
    nssv18759345RemappedPerfectNC_000001.10:g.236
    894241_236894325in
    v
    GRCh37.p13First PassNC_000001.10Chr1236,894,241236,894,325

    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)
    nssv187593459.3e-0526274654
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