A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436631



Internal ID215244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133023034..133023103hg38UCSC Ensembl
chr3:132741878..132741947hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436631
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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