A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10267n54



Internal ID20143691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:666450..667546hg38UCSC Ensembl
chr6:666450..667546hg19UCSC Ensembl
chr6:611450..612546hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600788, nsv600786, nsv600793, nsv600797, nsv600787, nsv600789
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10267n54
Frequency
Sample Size17421
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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