U.S. flag

An official website of the United States government

nsv5480372

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:202

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 22 studies. See in: genome view    
Submitted genomic117,647,119-117,647,320Question Mark
Overlapping variant regions from other studies: 124 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):117,287,173-117,287,374Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7117,647,119117,647,320
nsv5480372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7117,287,173117,287,374

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001706deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001706Submitted genomicNC_000007.14:g.117
647119_117647320de
l
GRCh38 (hg38)NC_000007.14Chr7117,647,119117,647,320
nssv17001706RemappedPerfectNC_000007.13:g.117
287173_117287374de
l
GRCh37.p13First PassNC_000007.13Chr7117,287,173117,287,374

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)
nssv17001706<0.00166404
Support Center