A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992456



Internal ID62433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4633176..4643704hg38UCSC Ensembl
chr7:4672807..4683335hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3810529
hg1910529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992456
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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