A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627087



Internal ID6667235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86402151..86406813hg38UCSC Ensembl
Innerchr11:86402201..86406763hg38UCSC Ensembl
Outerchr11:86402065..86406899hg38UCSC Ensembl
chr11:86113193..86117855hg19UCSC Ensembl
Innerchr11:86113243..86117805hg19UCSC Ensembl
Outerchr11:86113107..86117941hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg384663
hg194663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14221784
SamplesNA20805
Known GenesCCDC81
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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