A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532917



Internal ID308824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15420897..15423878hg38UCSC Ensembl
chr17:15324214..15327195hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382982
hg192982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532917
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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