A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274885



Internal ID1105
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585189, essv2585203
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)esv274885
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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