A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595659



Internal ID6982977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27121167..27127959hg38UCSC Ensembl
Innerchr3:27121667..27127459hg38UCSC Ensembl
Outerchr3:27120167..27128959hg38UCSC Ensembl
chr3:27162658..27169450hg19UCSC Ensembl
Innerchr3:27163158..27168950hg19UCSC Ensembl
Outerchr3:27161658..27170450hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386793
hg196793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10961119
SamplesNA18959
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595659
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