U.S. flag

An official website of the United States government

nsv5408255

  • 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: 118 SVs from 19 studies. See in: genome view    
Submitted genomic201,384,750-201,384,801Question Mark
Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):202,249,473-202,249,524Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2201,384,750201,384,801
nsv5408255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2202,249,473202,249,524

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923705alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923705Submitted genomicNC_000002.12:g.201
384750_201384801in
s280
GRCh38 (hg38)NC_000002.12Chr2201,384,750201,384,801
nssv16923705RemappedPerfectNC_000002.11:g.202
249473_202249524in
s280
GRCh37.p13First PassNC_000002.11Chr2202,249,473202,249,524

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)
nssv16923705<0.00146404
Support Center