A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440894



Internal ID219386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120243912..120244043hg38UCSC Ensembl
chr3:119962759..119962890hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938718
Samples
Known GenesGPR156
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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