A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275372



Internal ID1592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131535835..131536312hg38UCSC Ensembl
Outerchr11:131534305..131538273hg38UCSC Ensembl
Innerchr11:131405729..131406206hg19UCSC Ensembl
Outerchr11:131404199..131408167hg19UCSC Ensembl
Innerchr11:130910939..130911416hg18UCSC Ensembl
Outerchr11:130909409..130913377hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383969
hg193969
hg183969
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585538, essv2585783
Samples
Known GenesNTM
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275372
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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