A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1300n100



Internal ID19011668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132951557..133396436hg38UCSC Ensembl
chr11:132821452..133266331hg19UCSC Ensembl
chr11:132326662..132771541hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38444880
hg19444880
hg18444880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036912, nsv1038734, nsv1050386
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1300n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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