A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180735



Internal ID20747775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50046886..50048699hg38UCSC Ensembl
chr14:50513604..50515417hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg381814
hg191814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180735
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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