A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585867



Internal ID347446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25532393..25532518hg38UCSC Ensembl
Outerchr4:25531932..25535309hg38UCSC Ensembl
Innerchr4:25534015..25534140hg19UCSC Ensembl
Outerchr4:25533554..25536931hg19UCSC Ensembl
Innerchr4:25143113..25143238hg18UCSC Ensembl
Outerchr4:25142652..25146029hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275162
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)essv2585867
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer