A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196108



Internal ID20763148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3161768..3335002hg38UCSC Ensembl
chr16:3211769..3385002hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38173235
hg19173234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509422
Supporting Variants
Samples
Known GenesLINC00921, MEFV, OR1F1, OR1F2P, TIGD7, ZNF200, ZNF263, ZNF75A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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