A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1174n100



Internal ID20152790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55584048..55636296hg38UCSC Ensembl
chr11:55351524..55403772hg19UCSC Ensembl
chr11:55108100..55160348hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3852249
hg1952249
hg1852249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038504, nsv1045993, nsv1051534
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)dgv1174n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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