A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614783



Internal ID21806830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32395976..32396729hg38UCSC Ensembl
chr14:32865182..32865935hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038019
Supporting Variants
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614783
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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