A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1279n100



Internal ID20152895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112966837..112987859hg38UCSC Ensembl
chr11:112837559..112858581hg19UCSC Ensembl
chr11:112342769..112363791hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3821023
hg1921023
hg1821023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054170, nsv1042293
Samples
Known GenesNCAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1279n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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