A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436399



Internal ID215016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29114964..29143562hg38UCSC Ensembl
chr4:29116586..29145184hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3828599
hg1928599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436399
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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