A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1221n100



Internal ID20152837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67979689..68054143hg38UCSC Ensembl
chr11:67747160..67821610hg19UCSC Ensembl
chr11:67503736..67578186hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3874455
hg1974451
hg1874451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050471, nsv1046054, nsv1047567
Samples
Known GenesALDH3B1, CHKA, MIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1, UNC93B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1221n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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