A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666809



Internal ID9932914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:616697..616792hg38UCSC Ensembl
Outerchr5:616660..616842hg38UCSC Ensembl
Innerchr5:616812..616907hg19UCSC Ensembl
Outerchr5:616775..616957hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5749187
SamplesHG01083
Known GenesCEP72
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666809
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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