A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637836



Internal ID6677936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8550486..8582297hg38UCSC Ensembl
chr16:8600488..8632299hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831812
hg1931812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15370945
SamplesHG02721
Known GenesTMEM114
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637836
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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