A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665560



Internal ID9931665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58170117..58172238hg38UCSC Ensembl
chr16:58204021..58206142hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382122
hg192122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6386395, essv6592402, essv5755565, essv5598531
SamplesNA19684, NA12399, HG00250, HG00339
Known GenesCSNK2A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665560
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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