A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1296n100



Internal ID19011664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130552876..131171996hg38UCSC Ensembl
chr11:130422771..131041891hg19UCSC Ensembl
chr11:129927981..130547101hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38619121
hg19619121
hg18619121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043249, nsv1050318
Samples
Known GenesC11orf44, MIR8052, SNX19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1296n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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