A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933146



Internal ID22823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64896544..64896623hg38UCSC Ensembl
chr3:64882219..64882298hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443344
Supporting Variants
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933146
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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