A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275548



Internal ID1812606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26999200..27015172hg19UCSC Ensembl
Outerchr1:26997066..27025789hg19UCSC Ensembl
Innerchr1:26871787..26887759hg18UCSC Ensembl
Outerchr1:26869653..26898376hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv2586060
Samples
Known GenesARID1A
Method
AnalysisSV_analysis_a1
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee et al 2011
Pubmed ID21479260
Accession Number(s)esv275548
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer