A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7939n54



Internal ID22775834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:15310288..15450389hg38UCSC Ensembl
chr22:16527574..16667675hg19UCSC Ensembl
chr22:14907574..15047675hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38140102
hg19140102
hg18140102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588023, nsv588033
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7939n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer