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nsv4318621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,292,782

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 14773 SVs from 22 studies. See in: genome view    
Remapped(Score: Good):21,389,360-41,682,141Question Mark
Overlapping variant regions from other studies: 14772 SVs from 22 studies. See in: genome view    
Submitted genomic21,612,232-41,909,281Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4318621RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr221,389,36041,682,141
nsv4318621Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr221,612,23241,909,281

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091141inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091141RemappedGoodNC_000002.12:g.213
89360_41682141inv
GRCh38.p12First PassNC_000002.12Chr221,389,36041,682,141
nssv16091141Submitted genomicNC_000002.11:g.216
12232_41909281inv
GRCh37.p13NC_000002.11Chr221,612,23241,909,281

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)
nssv160911414.6e-005121694
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