A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038504



Internal ID19127723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55629481hg38UCSC Ensembl
Innerchr11:55351524..55396957hg19UCSC Ensembl
Innerchr11:55108100..55153533hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3845434
hg1945434
hg1845434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1174n100
Supporting Variantsnssv3510147
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)nsv1038504
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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