A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944286



Internal ID30193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196664827..196669828hg38UCSC Ensembl
chr3:196391698..196396699hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944286
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010462


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