A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585474



Internal ID367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81171620..81173084hg38UCSC Ensembl
Outerchr15:81171042..81173638hg38UCSC Ensembl
Innerchr15:81463961..81465425hg19UCSC Ensembl
Outerchr15:81463383..81465979hg19UCSC Ensembl
Innerchr15:79251016..79252480hg18UCSC Ensembl
Outerchr15:79250438..79253034hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382597
hg192597
hg182597
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275515
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585474
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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