A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196912



Internal ID20763952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79809470..79809829hg38UCSC Ensembl
chr15:80101812..80102171hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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