A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198807



Internal ID20765847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41336035..41337181hg38UCSC Ensembl
chr19:41841940..41843086hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381147
hg191147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530613
Supporting Variants
Samples
Known GenesTGFB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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