A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198495



Internal ID20765535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21972962..21974011hg38UCSC Ensembl
chr19:22155764..22156813hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531416
Supporting Variants
Samples
Known GenesZNF208
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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