A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275087



Internal ID1307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87881529..87881536hg38UCSC Ensembl
Outerchr10:87872753..87883091hg38UCSC Ensembl
Innerchr10:89641286..89641293hg19UCSC Ensembl
Outerchr10:89632510..89642848hg19UCSC Ensembl
Innerchr10:89631266..89631273hg18UCSC Ensembl
Outerchr10:89622490..89632828hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810339
hg1910339
hg1810339
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585521, essv2585463
Samples
Known GenesPTEN
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275087
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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