A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533470



Internal ID21857826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11424638..11425799hg38UCSC Ensembl
chr3:11466112..11467273hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991452
Supporting Variants
Samples
Known GenesATG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533470
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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