A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5887613



Internal ID8865016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119649385..119652407hg38UCSC Ensembl
Outerchr11:119649228..119652560hg38UCSC Ensembl
Innerchr11:119520095..119523117hg19UCSC Ensembl
Outerchr11:119519938..119523270hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661826
Supporting Variants
SamplesHG01174
Known GenesPVRL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5887613
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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