A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6006291



Internal ID8983694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15576056..15580566hg38UCSC Ensembl
chr16:15669913..15674423hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678976
Supporting Variants
SamplesNA18567
Known GenesC16orf45
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6006291
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