A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520464



Internal ID18818745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55636296hg38UCSC Ensembl
Innerchr11:55351524..55403772hg19UCSC Ensembl
Innerchr11:55108100..55160348hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3852249
hg1952249
hg1852249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051534
Supporting Variants
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520464
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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