A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633775



Internal ID7020581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23251882..23256035hg38UCSC Ensembl
Innerchr14:23251882..23256035hg38UCSC Ensembl
Outerchr14:23251382..23256535hg38UCSC Ensembl
chr14:23721091..23725244hg19UCSC Ensembl
Innerchr14:23721091..23725244hg19UCSC Ensembl
Outerchr14:23720591..23725744hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384154
hg194154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14935067
SamplesNA19315
Known GenesC14orf164
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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