A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516080



Internal ID292546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28226748..28226925hg38UCSC Ensembl
chr17:26553774..26553951hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712338
Samples
Known GenesPYY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516080
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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