A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5612578



Internal ID9670908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16611174..16617234hg38UCSC Ensembl
chr3:16652681..16658741hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386061
hg196061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665748
Supporting Variants
SamplesNA19399
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5612578
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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