A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633691



Internal ID7020499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20830695..20834129hg38UCSC Ensembl
Innerchr14:20830711..20834114hg38UCSC Ensembl
Outerchr14:20830680..20834145hg38UCSC Ensembl
chr14:21298854..21302288hg19UCSC Ensembl
Innerchr14:21298870..21302273hg19UCSC Ensembl
Outerchr14:21298839..21302304hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383435
hg193435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14925589
SamplesNA20904
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633691
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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