A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526212



Internal ID302350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28266884..28268907hg38UCSC Ensembl
chr17:26593910..26595933hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382024
hg192024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526212
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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