A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441239



Internal ID219720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25226329..25236925hg38UCSC Ensembl
chr4:25227951..25238547hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3810597
hg1910597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947035
Samples
Known GenesPI4K2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441239
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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