A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525684



Internal ID301834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66838293..66838352hg38UCSC Ensembl
chr17:64834411..64834470hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525684
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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