A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081975



Internal ID21991208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32454911..32454911hg38UCSC Ensembl
chr14:32924117..32924117hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600927
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081975
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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