A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633703



Internal ID7020510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21117087..21119231hg38UCSC Ensembl
Innerchr14:21117116..21119202hg38UCSC Ensembl
Outerchr14:21117058..21119260hg38UCSC Ensembl
chr14:21585246..21587390hg19UCSC Ensembl
Innerchr14:21585275..21587361hg19UCSC Ensembl
Outerchr14:21585217..21587419hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14926092, essv14926093
SamplesNA19917, HG01525
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633703
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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