A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521891



Internal ID298171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5058458..5063668hg38UCSC Ensembl
chr17:4961753..4966963hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521891
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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