A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617093



Internal ID21809140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36173578..36173578hg38UCSC Ensembl
chr14:36642784..36642784hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087940
Supporting Variants
Samples
Known GenesPTCSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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