A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616898



Internal ID7003784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36305229..36306045hg38UCSC Ensembl
Innerchr8:36305279..36305995hg38UCSC Ensembl
Outerchr8:36305179..36306095hg38UCSC Ensembl
chr8:36162747..36163563hg19UCSC Ensembl
Innerchr8:36162797..36163513hg19UCSC Ensembl
Outerchr8:36162697..36163613hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13168103
SamplesNA19054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616898
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