A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441196



Internal ID219678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188563394..188563529hg38UCSC Ensembl
chr3:188281182..188281317hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944075
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441196
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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