A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444087



Internal ID222469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162095157..162128324hg38UCSC Ensembl
chr3:161812945..161846112hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3833168
hg1933168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444087
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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