A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15936298



Internal ID3425578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76080534..76090732hg38UCSC Ensembl
Innerchr18:76080534..76090732hg38UCSC Ensembl
Outerchr18:76080034..76091232hg38UCSC Ensembl
chr18:73792489..73802687hg19UCSC Ensembl
Innerchr18:73792489..73802687hg19UCSC Ensembl
Outerchr18:73791989..73803187hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643158
Supporting Variants
SamplesHG03061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15936298
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