A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035489



Internal ID18778020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85791910..86067187hg38UCSC Ensembl
Innerchr11:85502953..85778229hg19UCSC Ensembl
Innerchr11:85180601..85455877hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38275278
hg19275277
hg18275277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503792
Samples
Known GenesCCDC83, PICALM, SYTL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035489
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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