A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274972



Internal ID347819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76192489..76192640hg38UCSC Ensembl
Outerchr15:76191001..76193195hg38UCSC Ensembl
Innerchr15:76484830..76484981hg19UCSC Ensembl
Outerchr15:76483342..76485536hg19UCSC Ensembl
Innerchr15:74271885..74272036hg18UCSC Ensembl
Outerchr15:74270397..74272591hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg382195
hg192195
hg182195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585980
Samples
Known GenesC15orf27
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274972
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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