A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032306



Internal ID21941649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20506307..20506988hg38UCSC Ensembl
chr14:20974466..20975147hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032306
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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