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nsv4209216

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:278,153

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 330 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):4,933,641-5,211,793Question Mark
Overlapping variant regions from other studies: 330 SVs from 19 studies. See in: genome view    
Submitted genomic4,954,871-5,233,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4209216RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr114,933,6415,211,793
nsv4209216Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr114,954,8715,233,023

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15798152deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15798152RemappedPerfectNC_000011.10:g.493
3641_5211793del
GRCh38.p12First PassNC_000011.10Chr114,933,6415,211,793
nssv15798152Submitted genomicNC_000011.9:g.4954
871_5233023del
GRCh37.p13NC_000011.9Chr114,954,8715,233,023

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)
nssv157981524.6e-005121694
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