A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636460



Internal ID7023254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51022337..51086008hg38UCSC Ensembl
chr15:51314534..51378205hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3863672
hg1963672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15248314
SamplesNA19000
Known GenesTNFAIP8L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636460
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer