A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155551



Internal ID22086056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9871658..9891794hg38UCSC Ensembl
Outerchr19:9870718..9894830hg38UCSC Ensembl
Innerchr19:9982334..10002470hg19UCSC Ensembl
Outerchr19:9981394..10005506hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824113
hg1924113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013452
Samples
Known GenesOLFM2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155551
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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