A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998891



Internal ID66837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79976325..80015598hg38UCSC Ensembl
chr7:79605641..79644914hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3839274
hg1939274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998891
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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