A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659878



Internal ID9579297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58169483..58171450hg38UCSC Ensembl
Outerchr16:58169446..58171500hg38UCSC Ensembl
Innerchr16:58203387..58205354hg19UCSC Ensembl
Outerchr16:58203350..58205404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6589571
SamplesNA18933
Known GenesCSNK2A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659878
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