A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626182



Internal ID6666331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46180891..46300218hg38UCSC Ensembl
chr11:46202442..46321769hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38119328
hg19119328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv197e214
Supporting Variantsessv14118986
SamplesHG02734
Known GenesCREB3L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626182
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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