A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633853



Internal ID7020659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26625031..26683599hg38UCSC Ensembl
chr14:27094237..27152805hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3858569
hg1958569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14946889, essv14946890
SamplesNA21144, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633853
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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