A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515180



Internal ID291666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53444956..53531260hg38UCSC Ensembl
chr17:51522317..51608621hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3886305
hg1986305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17713701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515180
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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