A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626443



Internal ID7013275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55572982..55596815hg38UCSC Ensembl
chr11:55340458..55364291hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3823834
hg1923834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14160437, essv14160435, essv14160434, essv14160436
SamplesHG03517, HG00346, NA19236, HG00371
Known GenesOR4C16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626443
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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