A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530477



Internal ID20903838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52519074..52847331hg38UCSC Ensembl
chr19:53022327..53350584hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38328258
hg19328258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198337
Samples
Known GenesZNF137P, ZNF28, ZNF468, ZNF600, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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