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nsv5522450

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:437

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 190 SVs from 29 studies. See in: genome view    
Submitted genomic2,320,032-2,320,468Question Mark
Overlapping variant regions from other studies: 190 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):2,223,326-2,223,762Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522450Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr172,320,0322,320,468
nsv5522450RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr172,223,3262,223,762

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17710909duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17710909Submitted genomicNC_000017.11:g.232
0032_2320468dup
GRCh38 (hg38)NC_000017.11Chr172,320,0322,320,468
nssv17710909RemappedPerfectNC_000017.10:g.222
3326_2223762dup
GRCh37.p13First PassNC_000017.10Chr172,223,3262,223,762

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)
nssv17710909<0.00116404
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