A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639509



Internal ID7026289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87299617..87360147hg38UCSC Ensembl
chr16:87333223..87393753hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3860531
hg1960531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555128
SamplesHG04107
Known GenesC16orf95, FBXO31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639509
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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