A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616309



Internal ID7003196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13376895..13391937hg38UCSC Ensembl
chr8:13234404..13249446hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3815043
hg1915043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13113933
SamplesHG02819
Known GenesDLC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616309
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer