A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2176n54



Internal ID20135600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107780369..107802574hg38UCSC Ensembl
chr11:107651095..107673300hg19UCSC Ensembl
chr11:107156305..107178510hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3822206
hg1922206
hg1822206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556385, nsv556386, nsv556383, nsv556388, nsv556384, nsv556387
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2176n54
Frequency
Sample Size17421
Observed Gain56
Observed Loss0
Observed Complex0
Frequencyn/a


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