A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639191



Internal ID6679286
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 Variantsdgv539e214
Supporting Variantsessv15528514, essv15528513
SamplesHG03100, HG02489
Known GenesWWOX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639191
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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