A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7851n54



Internal ID19000027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41870944..41897914hg38UCSC Ensembl
chr21:43291053..43318023hg19UCSC Ensembl
chr21:42164122..42191092hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826971
hg1926971
hg1826971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587571, nsv587573, nsv587569
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7851n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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