A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525965



Internal ID20899326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21012876..21595531hg38UCSC Ensembl
chr19:21195682..21778333hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38582656
hg19582652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198453
Samples
Known GenesLINC00664, ZNF429, ZNF430, ZNF431, ZNF493, ZNF708, ZNF714, ZNF738
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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