A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6524817



Internal ID9576937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27147516..27147753hg38UCSC Ensembl
chr8:27005033..27005270hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2656830
Supporting Variants
SamplesNA19144
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6524817
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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