A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1025n100



Internal ID20152641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4637957..4650235hg38UCSC Ensembl
chr11:4659187..4671465hg19UCSC Ensembl
chr11:4615763..4628041hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3812279
hg1912279
hg1812279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053297, nsv1035551
Samples
Known GenesOR51D1, OR51E1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1025n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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