A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934761



Internal ID22710092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52683530..52978765hg38UCSC Ensembl
chr19:53186783..53482018hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38295236
hg19295236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402325
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934761
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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