A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634447



Internal ID7021250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48799384..48831496hg38UCSC Ensembl
chr14:49268587..49300699hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3832113
hg1932113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15004704
SamplesHG02278
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634447
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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