A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7022n54



Internal ID22774917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118123425..118124611hg38UCSC Ensembl
chr2:118881001..118882187hg19UCSC Ensembl
chr2:118597471..118598657hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381187
hg191187
hg181187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582771, nsv582773, nsv582772
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7022n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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