A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647799



Internal ID6687852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41511654..41543254hg38UCSC Ensembl
chr22:41907658..41939258hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3831601
hg1931601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16430129
SamplesNA19984
Known GenesACO2, POLR3H
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647799
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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