A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275276



Internal ID1812798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37876234..37876767hg19UCSC Ensembl
Outerchr17:37876203..37876806hg19UCSC Ensembl
Innerchr17:35129760..35130293hg18UCSC Ensembl
Outerchr17:35129729..35130332hg18UCSC Ensembl
Cytoband17q12
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 Variantsessv2585806
Samples
Known GenesERBB2
Method
AnalysisSV_analysis_a1
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee et al 2011
Pubmed ID21479260
Accession Number(s)esv275276
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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