A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616181



Internal ID7003068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9426806..9441798hg38UCSC Ensembl
Innerchr8:9427306..9441298hg38UCSC Ensembl
Outerchr8:9425806..9442798hg38UCSC Ensembl
chr8:9284316..9299308hg19UCSC Ensembl
Innerchr8:9284816..9298808hg19UCSC Ensembl
Outerchr8:9283316..9300308hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3814993
hg1914993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13095658, essv13095655, essv13095656, essv13095657
SamplesHG03556, HG03024, HG03451, HG02837
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616181
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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