A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037943



Internal ID18780474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133378872..133705405hg38UCSC Ensembl
Innerchr11:133248767..133575300hg19UCSC Ensembl
Innerchr11:132753977..133080510hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38326534
hg19326534
hg18326534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504445
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037943
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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