A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039932



Internal ID21949275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34635308..34658835hg38UCSC Ensembl
chr14:35104514..35128041hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3823528
hg1923528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039932
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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