U.S. flag

An official website of the United States government

nsv5546593

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
Submitted genomic116,232,251-116,232,285Question Mark
Overlapping variant regions from other studies: 100 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):118,994,530-118,994,564Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546593Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9116,232,251116,232,285
nsv5546593RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9118,994,530118,994,564

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028407insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028407Submitted genomicNC_000009.12:g.116
232251_116232285in
s325
GRCh38 (hg38)NC_000009.12Chr9116,232,251116,232,285
nssv17028407RemappedPerfectNC_000009.11:g.118
994530_118994564in
s325
GRCh37.p13First PassNC_000009.11Chr9118,994,530118,994,564

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)
nssv17028407<0.00116404
Support Center