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nsv4316382

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,373,802

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 7707 SVs from 28 studies. See in: genome view    
Remapped(Score: Good):22,112,004-30,485,805Question Mark
Overlapping variant regions from other studies: 7744 SVs from 28 studies. See in: genome view    
Submitted genomic22,466,414-30,881,792Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4316382RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2222,112,00430,485,805
nsv4316382Submitted genomicGRCh37.p13Primary AssemblyNC_000022.10Chr2222,466,41430,881,792

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091290inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091290RemappedGoodNC_000022.11:g.221
12004_30485805inv
GRCh38.p12First PassNC_000022.11Chr2222,112,00430,485,805
nssv16091290Submitted genomicNC_000022.10:g.224
66414_30881792inv
GRCh37.p13NC_000022.10Chr2222,466,41430,881,792

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)
nssv160912904.6e-005121694
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