A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5671163



Internal ID9799248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29884779..29887731hg38UCSC Ensembl
chr8:29742295..29745247hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382953
hg192953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672936
Supporting Variants
SamplesNA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5671163
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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