A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1022n100



Internal ID20152638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4217176..4368359hg38UCSC Ensembl
chr11:4238406..4389589hg19UCSC Ensembl
chr11:4194982..4346165hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38151184
hg19151184
hg18151184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035329, nsv1038978
Samples
Known GenesOR52B4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1022n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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