A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198984



Internal ID20766024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6344906..6345605hg38UCSC Ensembl
chr19:6344917..6345616hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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