A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634118



Internal ID7020922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38483074..38576352hg38UCSC Ensembl
Innerchr14:38483108..38576319hg38UCSC Ensembl
Outerchr14:38483041..38576386hg38UCSC Ensembl
chr14:38952278..39045556hg19UCSC Ensembl
Innerchr14:38952312..39045523hg19UCSC Ensembl
Outerchr14:38952245..39045590hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3893279
hg1993279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14972077
SamplesHG00117
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634118
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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