A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1225n100



Internal ID20152841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75226932..75348452hg38UCSC Ensembl
chr11:74937977..75059496hg19UCSC Ensembl
chr11:74615625..74737144hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38121521
hg19121520
hg18121520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036292, nsv1049887
Samples
Known GenesARRB1, MIR326, TPBGL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1225n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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