A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7934n54



Internal ID20141358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:15408473..15927765hg38UCSC Ensembl
chr22:16050252..16569490hg19UCSC Ensembl
chr22:14430252..14949490hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38519293
hg19519239
hg18519239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588012, nsv588005, nsv588006, nsv588008, nsv588007
Samples
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7934n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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