A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2685n223



Internal ID22805653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8995775..9128274hg38UCSC Ensembl
chr16:9089632..9222131hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38132500
hg19132500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6514599, nsv6502528
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2685n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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