A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv513e199



Internal ID22758286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87568509..87573574hg38UCSC Ensembl
chr16:87602115..87607180hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385066
hg195066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676632, esv2661138
SamplesNA19070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv513e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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