A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180595



Internal ID20747635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35316596..35338498hg38UCSC Ensembl
chr14:35785802..35807704hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3821903
hg1921903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482818
Supporting Variants
Samples
Known GenesPSMA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180595
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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