A curated catalogue of human genomic structural variation




Variant Details

Variant: esv32767



Internal ID1683889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19740189..19873082hg19UCSC Ensembl
Innerchr8:19784469..19917362hg18UCSC Ensembl
Innerchr8:19784469..19917362hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg19188914
hg18188914
hg17188914
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv100850
Samples21656
Known GenesLPL
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv32767
Frequency
Sample Size51
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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