A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998213



Internal ID66355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69078837..69094722hg38UCSC Ensembl
chr7:68543824..68559709hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3815886
hg1915886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998213
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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