A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510792



Internal ID287399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25561336..25563668hg38UCSC Ensembl
chr15:25806483..25808815hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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