A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516384



Internal ID292844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68196830..68196882hg38UCSC Ensembl
chr15:68489168..68489220hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703888
Samples
Known GenesCALML4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516384
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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