A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199049



Internal ID20766089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8058749..8083893hg38UCSC Ensembl
chr19:8123633..8148777hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3825145
hg1925145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515739
Supporting Variants
Samples
Known GenesCCL25, FBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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