A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1298n100



Internal ID20152914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131485121..131531985hg38UCSC Ensembl
chr11:131355015..131401879hg19UCSC Ensembl
chr11:130860225..130907089hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3846865
hg1946865
hg1846865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038589, nsv1039803
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1298n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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