A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627734



Internal ID7014562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111301550..111339735hg38UCSC Ensembl
chr11:111172275..111210460hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3838186
hg1938186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14286897
SamplesNA19700
Known GenesCOLCA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627734
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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