U.S. flag

An official website of the United States government

nsv5548361

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 26 studies. See in: genome view    
Submitted genomic65,228,623-65,228,623Question Mark
Overlapping variant regions from other studies: 135 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):65,694,306-65,694,306Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548361Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr165,228,62365,228,623
nsv5548361RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr165,694,30665,694,306

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904553insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904553Submitted genomicNC_000001.11:g.652
28623_65228624ins3
18
GRCh38 (hg38)NC_000001.11Chr165,228,62365,228,623
nssv16904553RemappedPerfectNC_000001.10:g.656
94306_65694307ins3
18
GRCh37.p13First PassNC_000001.10Chr165,694,30665,694,306

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)
nssv16904553<0.00116370
Support Center