A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518260



Internal ID294657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52783839..52784511hg38UCSC Ensembl
chr15:53076036..53076708hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702782
Samples
Known GenesONECUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518260
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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