A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606853



Internal ID21798900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94066584..94073163hg38UCSC Ensembl
chr14:94532930..94539509hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386580
hg196580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021364
Supporting Variants
Samples
Known GenesDDX24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606853
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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