A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635622



Internal ID18587217
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 StatusS
Merged Variantsnsv1023365
Supporting Variants
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)nssv3635622
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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