A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991420



Internal ID61692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:695417..697172hg38UCSC Ensembl
chr7:735054..736809hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381756
hg191756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470123
Supporting Variants
Samples
Known GenesPRKAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991420
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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