A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520494



Internal ID296821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58066438..58082595hg38UCSC Ensembl
chr19:58577806..58593962hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3816158
hg1916157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724413
Samples
Known GenesZNF135
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520494
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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