A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538207



Internal ID21862562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170430720..170430720hg38UCSC Ensembl
chr3:170148508..170148508hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079450
Supporting Variants
Samples
Known GenesCLDN11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538207
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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