A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087940



Internal ID21997173
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 StatusM
Merged Variants
Supporting Variantsnssv17617093
Samples
Known GenesPTCSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087940
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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