A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626617



Internal ID6666767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62952476..63021925hg38UCSC Ensembl
chr11:62719948..62789397hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3869450
hg1969450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv204e214
Supporting Variantsessv14182099
SamplesNA19375
Known GenesSLC22A6, SLC22A8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626617
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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