A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634728



Internal ID6674845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63484345..63486304hg38UCSC Ensembl
Innerchr14:63484345..63486304hg38UCSC Ensembl
Outerchr14:63484137..63486539hg38UCSC Ensembl
chr14:63951063..63953022hg19UCSC Ensembl
Innerchr14:63951063..63953022hg19UCSC Ensembl
Outerchr14:63950855..63953257hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15040287
SamplesNA19064
Known GenesPPP2R5E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634728
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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