A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13118938



Internal ID4154701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15889214..15901196hg38UCSC Ensembl
Innerchr8:15889214..15901196hg38UCSC Ensembl
Outerchr8:15888714..15901696hg38UCSC Ensembl
chr8:15746723..15758705hg19UCSC Ensembl
Innerchr8:15746723..15758705hg19UCSC Ensembl
Outerchr8:15746223..15759205hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3811983
hg1911983
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616416
Supporting Variants
SamplesHG03757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13118938
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