A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193205



Internal ID20760245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1336430..1451010hg38UCSC Ensembl
chr16:1386431..1501011hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38114581
hg19114581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514311
Supporting Variants
Samples
Known GenesBAIAP3, C16orf91, CCDC154, CLCN7, GNPTG, TSR3, UNKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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