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nsv5449147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 15 studies. See in: genome view    
Submitted genomic222,259,899-222,259,954Question Mark
Overlapping variant regions from other studies: 106 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):223,124,618-223,124,673Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2222,259,899222,259,954
nsv5449147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2223,124,618223,124,673

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923920duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923920Submitted genomicNC_000002.12:g.222
259899_222259954du
p
GRCh38 (hg38)NC_000002.12Chr2222,259,899222,259,954
nssv16923920RemappedPerfectNC_000002.11:g.223
124618_223124673du
p
GRCh37.p13First PassNC_000002.11Chr2223,124,618223,124,673

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)
nssv16923920<0.00136400
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