A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1743n54



Internal ID20135167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34620946..34759389hg38UCSC Ensembl
chr11:34642493..34780936hg19UCSC Ensembl
chr11:34599069..34737512hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38138444
hg19138444
hg18138444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553998, nsv554000, nsv553999
Samples
Known GenesEHF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1743n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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