A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11200152



Internal ID4721219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162292556..162308343hg38UCSC Ensembl
Innerchr3:162292587..162308313hg38UCSC Ensembl
Outerchr3:162292526..162308374hg38UCSC Ensembl
chr3:162010344..162026131hg19UCSC Ensembl
Innerchr3:162010375..162026101hg19UCSC Ensembl
Outerchr3:162010314..162026162hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3815788
hg1915788
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598431
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11200152
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