A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602423



Internal ID21794470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64473157..64473157hg38UCSC Ensembl
chr14:64939875..64939875hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094228
Supporting Variants
Samples
Known GenesAKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602423
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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