A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616306



Internal ID7003193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13324359..13390732hg38UCSC Ensembl
Innerchr8:13324359..13390732hg38UCSC Ensembl
Outerchr8:13324155..13390996hg38UCSC Ensembl
chr8:13181868..13248241hg19UCSC Ensembl
Innerchr8:13181868..13248241hg19UCSC Ensembl
Outerchr8:13181664..13248505hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3866374
hg1966374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1378e214
Supporting Variantsessv13113929
SamplesHG02819
Known GenesDLC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616306
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