A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089305



Internal ID21998538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28759571..28759571hg38UCSC Ensembl
chr14:29228777..29228777hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089305
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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