A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7096n54



Internal ID22774991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145378051..145466590hg38UCSC Ensembl
chr2:146135619..146224158hg19UCSC Ensembl
chr2:145852089..145940628hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3888540
hg1988540
hg1888540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583249, nsv583248
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7096n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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