A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015236



Internal ID18757770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185775018..186082920hg38UCSC Ensembl
Innerchr4:186696172..187004074hg19UCSC Ensembl
Innerchr4:186933166..187241068hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38307903
hg19307903
hg18307903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635627
Samples
Known GenesSORBS2, TLR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015236
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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