A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941196



Internal ID28172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151745838..151757949hg38UCSC Ensembl
chr3:151463626..151475737hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3812112
hg1912112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440595
Supporting Variants
Samples
Known GenesAADACL2, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941196
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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