A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647284



Internal ID6687339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19985583..20137122hg38UCSC Ensembl
chr22:19973106..20124645hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38151540
hg19151540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16370120
SamplesHG00141
Known GenesARVCF, DGCR8, MIR1306, MIR185, MIR3618, MIR6816, RANBP1, TANGO2, TRMT2A, ZDHHC8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647284
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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