A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626184



Internal ID6666333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46295459..46319508hg38UCSC Ensembl
chr11:46317010..46341059hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3824050
hg1924050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14118990
SamplesHG02734
Known GenesCREB3L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626184
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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