A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1023n100



Internal ID20152639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4234887..4396971hg38UCSC Ensembl
chr11:4256117..4418201hg19UCSC Ensembl
chr11:4212693..4374777hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38162085
hg19162085
hg18162085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052915, nsv1036096, nsv1037093
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1023n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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