A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195536



Internal ID20762576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81064401..81219800hg38UCSC Ensembl
chr16:81098006..81253405hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38155400
hg19155400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501740
Supporting Variants
Samples
Known GenesC16orf46, GCSH, PKD1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02776


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