A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442334



Internal ID220762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57170869..57187817hg38UCSC Ensembl
chr3:57204897..57221845hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3816949
hg1916949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442334
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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