A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155635



Internal ID22086140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57479144..57491596hg38UCSC Ensembl
Outerchr19:57477028..57492505hg38UCSC Ensembl
Innerchr19:57990512..58002964hg19UCSC Ensembl
Outerchr19:57988396..58003873hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815478
hg1915478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013737
Samples
Known GenesZNF419, ZNF772
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155635
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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