A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512732



Internal ID18811013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63070597..63116730hg38UCSC Ensembl
Innerchr11:62838069..62884202hg19UCSC Ensembl
Innerchr11:62594645..62640778hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3846134
hg1946134
hg1846134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046221
Supporting Variants
Samples
Known GenesSLC22A24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512732
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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