A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1154n100



Internal ID22787241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54762047..54941169hg38UCSC Ensembl
chr11:51176562..51357233hg19UCSC Ensembl
chr11:51033138..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38179123
hg19180672
hg18180672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049838, nsv1054299, nsv1052109, nsv1054014, nsv1050539
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1154n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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