A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5722784



Internal ID9890570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62017584..62017896hg38UCSC Ensembl
chr8:62930143..62930455hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668936
Supporting Variants
SamplesNA20770
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5722784
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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