A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585354



Internal ID346933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25809748..25809778hg38UCSC Ensembl
Outerchr15:25809653..25813049hg38UCSC Ensembl
Innerchr15:26054895..26054925hg19UCSC Ensembl
Outerchr15:26054800..26058196hg19UCSC Ensembl
Innerchr15:23605988..23606018hg18UCSC Ensembl
Outerchr15:23605893..23609289hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg383397
hg193397
hg183397
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275525
Supporting Variants
Samples
Known GenesATP10A
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585354
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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