A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15076902



Internal ID5417883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80090401..80096266hg38UCSC Ensembl
Innerchr14:80090404..80096263hg38UCSC Ensembl
Outerchr14:80090398..80096269hg38UCSC Ensembl
chr14:80556744..80562609hg19UCSC Ensembl
Innerchr14:80556747..80562606hg19UCSC Ensembl
Outerchr14:80556741..80562612hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg385866
hg195866
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635062
Supporting Variants
SamplesNA18950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15076902
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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