A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633688



Internal ID6673809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20684511..20707081hg38UCSC Ensembl
Innerchr14:20684511..20707081hg38UCSC Ensembl
Outerchr14:20684011..20707581hg38UCSC Ensembl
chr14:21152670..21175240hg19UCSC Ensembl
Innerchr14:21152670..21175240hg19UCSC Ensembl
Outerchr14:21152170..21175740hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3822571
hg1922571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14924343
SamplesNA21117
Known GenesANG, RNASE4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633688
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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