A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275002



Internal ID347908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69038933..69039020hg38UCSC Ensembl
Outerchr15:69037475..69045323hg38UCSC Ensembl
Innerchr15:69331273..69331360hg19UCSC Ensembl
Outerchr15:69329815..69337663hg19UCSC Ensembl
Innerchr15:67118327..67118414hg18UCSC Ensembl
Outerchr15:67116869..67124717hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387849
hg197849
hg187849
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585846, essv2585398
Samples
Known GenesMIR548H4, NOX5
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275002
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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