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nsv4331174

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,970,295

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 14662 SVs from 22 studies. See in: genome view    
Remapped(Score: Good):35,914,916-52,885,210Question Mark
Overlapping variant regions from other studies: 14660 SVs from 22 studies. See in: genome view    
Submitted genomic36,139,982-53,112,348Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4331174RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr235,914,91652,885,210
nsv4331174Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr236,139,98253,112,348

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091146inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091146RemappedGoodNC_000002.12:g.359
14916_52885210inv
GRCh38.p12First PassNC_000002.12Chr235,914,91652,885,210
nssv16091146Submitted genomicNC_000002.11:g.361
39982_53112348inv
GRCh37.p13NC_000002.11Chr236,139,98253,112,348

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)
nssv160911464.6e-005121694
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