A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993094



Internal ID62856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15202682..15273245hg38UCSC Ensembl
chr7:15242307..15312870hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3870564
hg1970564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462637
Supporting Variants
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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