A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616842



Internal ID7003728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33733505..33734233hg38UCSC Ensembl
Innerchr8:33733528..33734211hg38UCSC Ensembl
Outerchr8:33733483..33734256hg38UCSC Ensembl
chr8:33591023..33591751hg19UCSC Ensembl
Innerchr8:33591046..33591729hg19UCSC Ensembl
Outerchr8:33591001..33591774hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13161533
SamplesHG02028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616842
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