A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6249569



Internal ID9759888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68650341..68653273hg38UCSC Ensembl
chr16:68684244..68687176hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382933
hg192933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668844
Supporting Variants
SamplesNA19713
Known GenesCDH3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6249569
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