A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183189



Internal ID20750229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90948900..91372817hg38UCSC Ensembl
chr14:91415244..91839161hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38423918
hg19423918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511480
Supporting Variants
Samples
Known GenesC14orf159, CCDC88C, GPR68, RPS6KA5, SNORA11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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