A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5426857



Internal ID8404260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67788283..67791044hg38UCSC Ensembl
chr16:67822186..67824947hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382762
hg192762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662518
Supporting Variants
SamplesNA19235
Known GenesRANBP10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5426857
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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