A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516120



Internal ID292585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47065024..47065201hg38UCSC Ensembl
chr19:47568281..47568458hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723734
Samples
Known GenesZC3H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516120
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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