A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531059



Internal ID307021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52599659..52946366hg38UCSC Ensembl
chr19:53102912..53449619hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38346708
hg19346708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724192
Samples
Known GenesZNF137P, ZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF816-ZNF321P, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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