A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634702



Internal ID7021505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62166820..62324145hg38UCSC Ensembl
Innerchr14:62166970..62323995hg38UCSC Ensembl
Outerchr14:62166670..62324295hg38UCSC Ensembl
chr14:62633538..62790863hg19UCSC Ensembl
Innerchr14:62633688..62790713hg19UCSC Ensembl
Outerchr14:62633388..62791013hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38157326
hg19157326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv403e214
Supporting Variantsessv15036747, essv15036746
SamplesHG00851, HG02166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634702
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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