A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639512



Internal ID7026292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87320763..87352951hg38UCSC Ensembl
chr16:87354369..87386557hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3832189
hg1932189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555132
SamplesHG04107
Known GenesFBXO31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639512
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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