A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635062



Internal ID7021862
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15076902, essv15076903
SamplesNA19920, NA18950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635062
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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