A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7818n54



Internal ID20141242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33321856..33324562hg38UCSC Ensembl
chr21:34694161..34696867hg19UCSC Ensembl
chr21:33616031..33618737hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382707
hg192707
hg182707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587393, nsv587391, nsv587382, nsv587383
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7818n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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