A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635323



Internal ID7022122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91105376..91106130hg38UCSC Ensembl
Innerchr14:91105384..91106123hg38UCSC Ensembl
Outerchr14:91105369..91106138hg38UCSC Ensembl
chr14:91571720..91572474hg19UCSC Ensembl
Innerchr14:91571728..91572467hg19UCSC Ensembl
Outerchr14:91571713..91572482hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15094284, essv15094283, essv15094282
SamplesNA18757, NA19000, NA18945
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635323
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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