A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635462



Internal ID7022261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98446440..98452696hg38UCSC Ensembl
Innerchr14:98446940..98452196hg38UCSC Ensembl
Outerchr14:98445440..98453696hg38UCSC Ensembl
chr14:98912777..98919033hg19UCSC Ensembl
Innerchr14:98913277..98918533hg19UCSC Ensembl
Outerchr14:98911777..98920033hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386257
hg196257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15106679
SamplesHG02678
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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