A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155555



Internal ID22086060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15173938..15241561hg38UCSC Ensembl
Outerchr19:15172350..15245581hg38UCSC Ensembl
Innerchr19:15284749..15352372hg19UCSC Ensembl
Outerchr19:15283161..15356392hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3873232
hg1973232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013456
Samples
Known GenesBRD4, EPHX3, MIR6795, NOTCH3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155555
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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