A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5536163



Internal ID8513566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89469832..89470883hg38UCSC Ensembl
Outerchr16:89469792..89470943hg38UCSC Ensembl
Innerchr16:89536240..89537291hg19UCSC Ensembl
Outerchr16:89536200..89537351hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665887
Supporting Variants
SamplesHG01047
Known GenesANKRD11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5536163
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer