A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1272n100



Internal ID22787359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106588947..106644047hg38UCSC Ensembl
chr11:106459674..106514773hg19UCSC Ensembl
chr11:105964884..106019983hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3855101
hg1955100
hg1855100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038836, nsv1054602
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1272n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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