A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998890



Internal ID66836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79972321..79990470hg38UCSC Ensembl
chr7:79601637..79619786hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3818150
hg1918150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998890
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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