A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510019



Internal ID18808300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133926415..133953490hg38UCSC Ensembl
Innerchr11:133796310..133823385hg19UCSC Ensembl
Innerchr11:133301520..133328595hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3827076
hg1927076
hg1827076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043506
Supporting Variants
Samples
Known GenesIGSF9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510019
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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