A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519125



Internal ID21843484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1091984..1965184hg38UCSC Ensembl
chr3:1133668..2006868hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38873201
hg19873201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990960
Supporting Variants
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519125
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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