A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1219n100



Internal ID20152835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67730549..67969010hg38UCSC Ensembl
chr11:67498020..67736481hg19UCSC Ensembl
chr11:67254596..67493057hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38238462
hg19238462
hg18238462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037810, nsv1044773, nsv1048822, nsv1041933, nsv1037306, nsv1044670
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1219n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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