A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088609



Internal ID4090425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34055442..34063970hg38UCSC Ensembl
Innerchr11:34055462..34063951hg38UCSC Ensembl
Outerchr11:34055423..34063990hg38UCSC Ensembl
chr11:34076989..34085517hg19UCSC Ensembl
Innerchr11:34077009..34085498hg19UCSC Ensembl
Outerchr11:34076970..34085537hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388529
hg198529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625904
Supporting Variants
SamplesHG02142
Known GenesCAPRIN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088609
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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