A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955536



Internal ID8932939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732691..89733030hg38UCSC Ensembl
chr16:89799099..89799438hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674443
Supporting Variants
SamplesHG00619
Known GenesZNF276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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