A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524893



Internal ID301078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37576053..37576256hg38UCSC Ensembl
chr17:35936151..35936354hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712917
Samples
Known GenesSYNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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