A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626214



Internal ID7013048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47884472..47889544hg38UCSC Ensembl
chr11:47906024..47911096hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385073
hg195073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14123811, essv14123810
SamplesHG00448, HG03575
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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