A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585979



Internal ID347558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155939239..155939953hg38UCSC Ensembl
Outerchr4:155935481..155941197hg38UCSC Ensembl
Innerchr4:156860391..156861105hg19UCSC Ensembl
Outerchr4:156856633..156862349hg19UCSC Ensembl
Innerchr4:157079841..157080555hg18UCSC Ensembl
Outerchr4:157076083..157081799hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385717
hg195717
hg185717
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274871
Supporting Variants
Samples
Known GenesCTSO
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585979
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