A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12062n54



Internal ID22779957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25113490..25134659hg38UCSC Ensembl
chr8:24971005..24992174hg19UCSC Ensembl
chr8:25026922..25048091hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3821170
hg1921170
hg1821170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610797, nsv610794, nsv610800
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12062n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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