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nsv7054624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,146

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 289 SVs from 46 studies. See in: genome view    
    Submitted genomic150,443,401-150,497,546Question Mark
    Overlapping variant regions from other studies: 289 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):150,140,489-150,194,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7150,443,401150,497,546
    nsv7054624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7150,140,489150,194,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782093inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782093Submitted genomicNC_000007.14:g.150
    443401_150497546in
    v
    GRCh38 (hg38)NC_000007.14Chr7150,443,401150,497,546
    nssv18782093RemappedPerfectNC_000007.13:g.150
    140489_150194634in
    v
    GRCh37.p13First PassNC_000007.13Chr7150,140,489150,194,634

    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)
    nssv187820932.5e-057274282
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