U.S. flag

An official website of the United States government

nsv5410347

  • 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: 108 SVs from 21 studies. See in: genome view    
Submitted genomic207,581,736-207,581,787Question Mark
Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):208,446,460-208,446,511Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410347Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2207,581,736207,581,787
nsv5410347RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2208,446,460208,446,511

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16924778alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16924778Submitted genomicNC_000002.12:g.207
581736_207581787in
s257
GRCh38 (hg38)NC_000002.12Chr2207,581,736207,581,787
nssv16924778RemappedPerfectNC_000002.11:g.208
446460_208446511in
s257
GRCh37.p13First PassNC_000002.11Chr2208,446,460208,446,511

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)
nssv16924778<0.00136404
Support Center