A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638936



Internal ID7025721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69839427..69921835hg38UCSC Ensembl
chr16:69873330..69955738hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3882409
hg1982409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503814
SamplesHG02079
Known GenesWWP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638936
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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