A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188323



Internal ID20755363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73229750..73230828hg38UCSC Ensembl
chr14:73696458..73697536hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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