A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933934



Internal ID23359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64705057..64708020hg38UCSC Ensembl
chr3:64690733..64693696hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg382964
hg192964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435104
Supporting Variants
Samples
Known GenesADAMTS9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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