A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7816n54



Internal ID20141240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33321856..33323970hg38UCSC Ensembl
chr21:34694161..34696275hg19UCSC Ensembl
chr21:33616031..33618145hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382115
hg192115
hg182115
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587386, nsv587381
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7816n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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