A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1088n100



Internal ID22787175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30872741..30907727hg38UCSC Ensembl
chr11:30894288..30929274hg19UCSC Ensembl
chr11:30850864..30885850hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3834987
hg1934987
hg1834987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045366, nsv1043222
Samples
Known GenesDCDC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1088n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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