A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585203



Internal ID96
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128471978..128472283hg38UCSC Ensembl
Outerchr11:128471847..128472432hg38UCSC Ensembl
Innerchr11:128341873..128342178hg19UCSC Ensembl
Outerchr11:128341742..128342327hg19UCSC Ensembl
Innerchr11:127847083..127847388hg18UCSC Ensembl
Outerchr11:127846952..127847537hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38586
hg19586
hg18586
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv274885
Supporting Variants
Samples
Known GenesETS1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585203
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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