A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv539e214



Internal ID20121962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78117264..78142432hg38UCSC Ensembl
chr16:78151161..78176329hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3825169
hg1925169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639191, esv3639192
SamplesHG03100, HG02489, NA19468
Known GenesWWOX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv539e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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