U.S. flag

An official website of the United States government

nsv5561184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
Submitted genomic123,216,076-123,216,127Question Mark
Overlapping variant regions from other studies: 82 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):125,978,355-125,978,406Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561184Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9123,216,076123,216,127
nsv5561184RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,978,355125,978,406

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027159sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027159Submitted genomicNC_000009.12:g.123
216076_123216127in
s361
GRCh38 (hg38)NC_000009.12Chr9123,216,076123,216,127
nssv17027159RemappedPerfectNC_000009.11:g.125
978355_125978406in
s361
GRCh37.p13First PassNC_000009.11Chr9125,978,355125,978,406

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)
nssv17027159<0.00126404
Support Center