A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146570



Internal ID345775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58414874..58496874hg38UCSC Ensembl
chr19:58926241..59008241hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3882001
hg1982001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724458
Samples
Known GenesZNF132, ZNF324, ZNF324B, ZNF446, ZNF584
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146570
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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