U.S. flag

An official website of the United States government

nsv5546352

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 360 SVs from 33 studies. See in: genome view    
Submitted genomic45,405,295-45,405,338Question Mark
Overlapping variant regions from other studies: 360 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):46,825,210-46,825,253Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546352Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2145,405,29545,405,338
nsv5546352RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2146,825,21046,825,253

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727214insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727214Submitted genomicNC_000021.9:g.4540
5295_45405338ins57
GRCh38 (hg38)NC_000021.9Chr2145,405,29545,405,338
nssv17727214RemappedPerfectNC_000021.8:g.4682
5210_46825253ins57
GRCh37.p13First PassNC_000021.8Chr2146,825,21046,825,253

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)
nssv177272140.2918446352
Support Center