A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032504



Internal ID89360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16808100..16978218hg38UCSC Ensembl
chr10:16850099..17020217hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38170119
hg19170119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481509
Supporting Variants
Samples
Known GenesCUBN, RSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032504
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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