U.S. flag

An official website of the United States government

nsv5562060

  • 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: 66 SVs from 21 studies. See in: genome view    
Submitted genomic21,663,185-21,663,236Question Mark
Overlapping variant regions from other studies: 66 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):22,131,398-22,131,449Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1421,663,18521,663,236
nsv5562060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1422,131,39822,131,449

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17695352sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17695352Submitted genomicNC_000014.9:g.2166
3185_21663236ins47
0
GRCh38 (hg38)NC_000014.9Chr1421,663,18521,663,236
nssv17695352RemappedPerfectNC_000014.8:g.2213
1398_22131449ins47
0
GRCh37.p13First PassNC_000014.8Chr1422,131,39822,131,449

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)
nssv17695352<0.00116404
Support Center