A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5701480



Internal ID8965826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:805905..806965hg38UCSC Ensembl
Outerchr11:805868..807015hg38UCSC Ensembl
Innerchr11:805905..806965hg19UCSC Ensembl
Outerchr11:805868..807015hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665829
Supporting Variants
SamplesHG00536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5701480
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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