A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433557



Internal ID212269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32460253..32473992hg38UCSC Ensembl
chr1:32925854..32939593hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3813740
hg1913740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903625
Samples
Known GenesZBTB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433557
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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