A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533998



Internal ID20907359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19978285..20619766hg38UCSC Ensembl
chr19:20089094..20802572hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38641482
hg19713479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3460n223
Supporting Variantsnssv18198393
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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