A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670517



Internal ID9589936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89591867..89592610hg38UCSC Ensembl
chr16:89658275..89659018hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6415515
SamplesNA19313
Known GenesCPNE7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670517
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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