U.S. flag

An official website of the United States government

nsv5487587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,694

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 238 SVs from 28 studies. See in: genome view    
Submitted genomic15,218,888-15,221,581Question Mark
Overlapping variant regions from other studies: 244 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):15,218,886-15,221,579Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr915,218,88815,221,581
nsv5487587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr915,218,88615,221,579

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17020583deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17020583Submitted genomicNC_000009.12:g.152
18888_15221581del
GRCh38 (hg38)NC_000009.12Chr915,218,88815,221,581
nssv17020583RemappedPerfectNC_000009.11:g.152
18886_15221579del
GRCh37.p13First PassNC_000009.11Chr915,218,88615,221,579

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)
nssv17020583<0.00116404
Support Center