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nsv5437627

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:427

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
Submitted genomic167,446,066-167,446,492Question Mark
Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):167,163,854-167,164,280Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3167,446,066167,446,492
nsv5437627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3167,163,854167,164,280

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942409deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942409Submitted genomicNC_000003.12:g.167
446066_167446492de
l
GRCh38 (hg38)NC_000003.12Chr3167,446,066167,446,492
nssv16942409RemappedPerfectNC_000003.11:g.167
163854_167164280de
l
GRCh37.p13First PassNC_000003.11Chr3167,163,854167,164,280

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)
nssv16942409<0.00116404
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