A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548655



Internal ID21873010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67593226..67593355hg38UCSC Ensembl
chr3:67643650..67643779hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993908
Supporting Variants
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548655
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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