A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530982



Internal ID306948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58411830..58451891hg38UCSC Ensembl
chr19:58923197..58963258hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3840062
hg1940062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724457
Samples
Known GenesZNF132, ZNF324B, ZNF584
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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