A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14047498



Internal ID5889591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21135401..21286053hg38UCSC Ensembl
chr11:21156947..21307599hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38150653
hg19150653
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625566
Supporting Variants
SamplesNA19312
Known GenesNELL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14047498
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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