A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633895



Internal ID7020699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27990251..28053436hg38UCSC Ensembl
chr14:28459457..28522642hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3863186
hg1963186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv390e214
Supporting Variantsessv14949888, essv14949887, essv14949886, essv14949889
SamplesHG03960, HG03792, HG02651, HG03681
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633895
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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