A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618536



Internal ID7005418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116363892..116372573hg38UCSC Ensembl
Innerchr8:116363929..116372536hg38UCSC Ensembl
Outerchr8:116363855..116372610hg38UCSC Ensembl
chr8:117376130..117384811hg19UCSC Ensembl
Innerchr8:117376167..117384774hg19UCSC Ensembl
Outerchr8:117376093..117384848hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg388682
hg198682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13300549
SamplesHG02888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618536
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