A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434686



Internal ID15281640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35600759..35602457hg38UCSC Ensembl
Innerchr22:35601457..35601759hg38UCSC Ensembl
Outerchr22:35599759..35603457hg38UCSC Ensembl
chr22:35996806..35998504hg19UCSC Ensembl
Innerchr22:35997504..35997806hg19UCSC Ensembl
Outerchr22:35995806..35999504hg19UCSC Ensembl
chr22:34326752..34328450hg18UCSC Ensembl
Innerchr22:34327752..34327450hg18UCSC Ensembl
Outerchr22:34325752..34329450hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2614e59
Supporting Variantsessv8693302
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434686
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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