A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520902



Internal ID297211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41654942..41654993hg38UCSC Ensembl
chr17:39811194..39811245hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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