A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155615



Internal ID22086120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53425511..53511924hg38UCSC Ensembl
Outerchr19:53422400..53513852hg38UCSC Ensembl
Innerchr19:53928764..54015178hg19UCSC Ensembl
Outerchr19:53925653..54017106hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3891453
hg1991454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013703
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155615
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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