A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520480



Internal ID296807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12527466..12527584hg38UCSC Ensembl
chr19:12638280..12638398hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721514
Samples
Known GenesZNF564
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520480
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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