A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509198



Internal ID18460793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129228206..129415243hg38UCSC Ensembl
Innerchr11:129098101..129285138hg19UCSC Ensembl
Innerchr11:128603311..128790348hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38187038
hg19187038
hg18187038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046731
Supporting Variants
Samples
Known GenesBARX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509198
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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