A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528258



Internal ID304323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39409499..39412022hg38UCSC Ensembl
chr19:39900139..39902662hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723334
Samples
Known GenesMIR4530
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528258
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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