A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198397



Internal ID20765437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20066201..20618500hg38UCSC Ensembl
chr19:20177010..20801306hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38552300
hg19624297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527143
Supporting Variants
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF737, ZNF826P, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00038


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