A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082512



Internal ID21991745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24325222..24325222hg38UCSC Ensembl
chr14:24794428..24794428hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598488
Samples
Known GenesADCY4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082512
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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