A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638198



Internal ID6678296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22121308..22167549hg38UCSC Ensembl
chr16:22132629..22178870hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3846242
hg1946242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15416373, essv15416372
SamplesHG01094, NA21120
Known GenesVWA3A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638198
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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