A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524901



Internal ID301086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78201461..78211996hg38UCSC Ensembl
chr17:76197542..76208077hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3810536
hg1910536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714837
Samples
Known GenesAFMID
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524901
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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