A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676833



Internal ID9942938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59392910..59393020hg38UCSC Ensembl
chr16:59426814..59426924hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6044436, essv5434693, essv6098033
SamplesNA18502, NA19238, NA19240
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676833
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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