A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2367e59



Internal ID22763587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237211370..237213468hg38UCSC Ensembl
chr2:238120013..238122111hg19UCSC Ensembl
chr2:237784752..237786850hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3399556, esv3330010
SamplesNA19238, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2367e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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