A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606791



Internal ID21798838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32784104..32784104hg38UCSC Ensembl
chr14:33253310..33253310hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098141
Supporting Variants
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606791
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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