A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13270910



Internal ID3272726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102558699..102560292hg38UCSC Ensembl
Innerchr8:102558700..102560292hg38UCSC Ensembl
Outerchr8:102558699..102560293hg38UCSC Ensembl
chr8:103570927..103572520hg19UCSC Ensembl
Innerchr8:103570928..103572520hg19UCSC Ensembl
Outerchr8:103570927..103572521hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3618226
Supporting Variants
SamplesNA19119
Known GenesODF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13270910
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