A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1215n100



Internal ID20152831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67705434..67981775hg38UCSC Ensembl
chr11:67472905..67749246hg19UCSC Ensembl
chr11:67229481..67505822hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38276342
hg19276342
hg18276342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049673, nsv1045331, nsv1046044, nsv1048589, nsv1044800, nsv1042696, nsv1047985, nsv1043580, nsv1052363
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)dgv1215n100
Frequency
Sample Size29084
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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