A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013452



Internal ID22075083
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155551
Supporting Variants
Samples
Known GenesOLFM2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013452
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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