A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528024



Internal ID304097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36018042..36084494hg38UCSC Ensembl
chr19:36508944..36575396hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3866453
hg1966453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723057
Samples
Known GenesCLIP3, THAP8, WDR62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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