A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616687



Internal ID7003573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25654477..25738502hg38UCSC Ensembl
chr8:25511993..25596018hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3884026
hg1984026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13147674, essv13147675
SamplesNA20274, NA19625
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616687
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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