A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627650



Internal ID7014478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107465318..107477475hg38UCSC Ensembl
Innerchr11:107465319..107477475hg38UCSC Ensembl
Outerchr11:107465318..107477476hg38UCSC Ensembl
chr11:107336044..107348201hg19UCSC Ensembl
Innerchr11:107336045..107348201hg19UCSC Ensembl
Outerchr11:107336044..107348202hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812158
hg1912158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14276666, essv14276675, essv14276673, essv14276664, essv14276665, essv14276676, essv14276662, essv14276668, essv14276677, essv14276663, essv14276672, essv14276679, essv14276674, essv14276670, essv14276669, essv14276678, essv14276671, essv14276667
SamplesHG01986, NA19700, NA20356, NA20287, HG02461, NA20412, HG02009, NA19210, HG02511, HG01889, HG03024, NA19436, HG02667, HG03539, NA20357, HG03258, HG03351, HG03077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627650
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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