A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635386



Internal ID7022185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94670510..94675828hg38UCSC Ensembl
Innerchr14:94670510..94675828hg38UCSC Ensembl
Outerchr14:94670010..94676328hg38UCSC Ensembl
chr14:95136847..95142165hg19UCSC Ensembl
Innerchr14:95136847..95142165hg19UCSC Ensembl
Outerchr14:95136347..95142665hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385319
hg195319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103231
SamplesNA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635386
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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