A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639579



Internal ID6679670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89428478..89441377hg38UCSC Ensembl
chr16:89494886..89507785hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569817
SamplesNA21108
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639579
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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