A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434434



Internal ID213109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122390965..122407947hg38UCSC Ensembl
chr3:122109812..122126794hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3816983
hg1916983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939485
Samples
Known GenesFAM162A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434434
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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