A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676847



Internal ID9596266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89634763..89635008hg38UCSC Ensembl
chr16:89701171..89701416hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5399497, essv5789960, essv6109110
SamplesHG01516, NA19789, NA20287
Known GenesDPEP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676847
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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