A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711716



Internal ID135382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15643000..15675111hg38UCSC Ensembl
chr17:15546314..15578425hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3832112
hg1932112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520587
Supporting Variants
Samples
Known GenesTRIM16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711716
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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