A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7876n54



Internal ID19000052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43739631..43743809hg38UCSC Ensembl
chr21:45159512..45163690hg19UCSC Ensembl
chr21:43983940..43988118hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384179
hg194179
hg184179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587714, nsv587709, nsv587708
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7876n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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