A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023365



Internal ID18765898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185477063..185594299hg38UCSC Ensembl
Innerchr4:186398217..186515453hg19UCSC Ensembl
Innerchr4:186635211..186752447hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38117237
hg19117237
hg18117237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5493n100
Supporting Variantsnssv3635622, nssv3635623
Samples
Known GenesPDLIM3, SORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023365
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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