A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633704



Internal ID7020511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21150573..21164581hg38UCSC Ensembl
Innerchr14:21150573..21164581hg38UCSC Ensembl
Outerchr14:21150073..21165081hg38UCSC Ensembl
chr14:21618732..21632740hg19UCSC Ensembl
Innerchr14:21618732..21632740hg19UCSC Ensembl
Outerchr14:21618232..21633240hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3814009
hg1914009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14926094
SamplesHG01524
Known GenesOR5AU1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633704
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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