A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515532



Internal ID292014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49369411..49379213hg38UCSC Ensembl
chr19:49872668..49882470hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg389803
hg199803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723995
Samples
Known GenesDKKL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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