A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090158



Internal ID21999391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23203471..23203471hg38UCSC Ensembl
chr14:23672680..23672680hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090158
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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