A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032274



Internal ID21941617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73501126..73502553hg38UCSC Ensembl
chr14:73967830..73969257hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611898
Samples
Known GenesHEATR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032274
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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