U.S. flag

An official website of the United States government

nsv5550268

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
Submitted genomic222,266,496-222,266,528Question Mark
Overlapping variant regions from other studies: 107 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):223,131,215-223,131,247Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5550268Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2222,266,496222,266,528
nsv5550268RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2223,131,215223,131,247

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923923insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923923Submitted genomicNC_000002.12:g.222
266496_222266528in
s319
GRCh38 (hg38)NC_000002.12Chr2222,266,496222,266,528
nssv16923923RemappedPerfectNC_000002.11:g.223
131215_223131247in
s319
GRCh37.p13First PassNC_000002.11Chr2223,131,215223,131,247

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)
nssv169239230.003186404
Support Center