A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1285n100



Internal ID22787372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119896905..119918974hg38UCSC Ensembl
chr11:119767614..119789683hg19UCSC Ensembl
chr11:119272824..119294893hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3822070
hg1922070
hg1822070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044698, nsv1051760
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)dgv1285n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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