A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626691



Internal ID7013522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66250983..66254888hg38UCSC Ensembl
Innerchr11:66250989..66254882hg38UCSC Ensembl
Outerchr11:66250977..66254894hg38UCSC Ensembl
chr11:66018454..66022359hg19UCSC Ensembl
Innerchr11:66018460..66022353hg19UCSC Ensembl
Outerchr11:66018448..66022365hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383906
hg193906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14194639
SamplesNA18504
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626691
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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