A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1090n100



Internal ID22787177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31600987..31673444hg38UCSC Ensembl
chr11:31622534..31694992hg19UCSC Ensembl
chr11:31579110..31651568hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3872458
hg1972459
hg1872459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043011, nsv1038042, nsv1052305, nsv1046402, nsv1049999
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1090n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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