A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627655



Internal ID6667802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107740978..107953197hg38UCSC Ensembl
Innerchr11:107741128..107953047hg38UCSC Ensembl
Outerchr11:107740828..107953347hg38UCSC Ensembl
chr11:107611704..107823923hg19UCSC Ensembl
Innerchr11:107611854..107823773hg19UCSC Ensembl
Outerchr11:107611554..107824073hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38212220
hg19212220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14276853, essv14276852
SamplesHG03645, HG02049
Known GenesRAB39A, SLC35F2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627655
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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