A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13168103



Internal ID5621278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36305229..36306045hg38UCSC Ensembl
Innerchr8:36305279..36305995hg38UCSC Ensembl
Outerchr8:36305179..36306095hg38UCSC Ensembl
chr8:36162747..36163563hg19UCSC Ensembl
Innerchr8:36162797..36163513hg19UCSC Ensembl
Outerchr8:36162697..36163613hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616898
Supporting Variants
SamplesNA19054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13168103
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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