A curated catalogue of human genomic structural variation




Variant Details

Variant: esv33876



Internal ID1683225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:33957191..33957359hg19UCSC Ensembl
Innerchr5:33992948..33993116hg18UCSC Ensembl
Innerchr5:33992948..33993116hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg191027
hg181027
hg171027
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv98915
Samples21606
Known GenesSLC45A2
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv33876
Frequency
Sample Size51
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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