A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039609



Internal ID21948952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36411642..36414028hg38UCSC Ensembl
chr14:36880847..36883233hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg382387
hg192387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039609
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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