A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181864



Internal ID20748904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67315407..67315740hg38UCSC Ensembl
chr16:67349310..67349643hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506984
Supporting Variants
Samples
Known GenesKCTD19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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