A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474268



Internal ID251929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37448925..37448984hg38UCSC Ensembl
chr9:37448922..37448981hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024758
Samples
Known GenesZBTB5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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