A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626864



Internal ID7013694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76162412..76188888hg38UCSC Ensembl
chr11:75873456..75899932hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3826477
hg1926477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214077
SamplesHG02299
Known GenesWNT11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626864
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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