A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2586025



Internal ID347604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122149091..122149294hg38UCSC Ensembl
Outerchr11:122143902..122151817hg38UCSC Ensembl
Innerchr11:122019799..122020002hg19UCSC Ensembl
Outerchr11:122014610..122022525hg19UCSC Ensembl
Innerchr11:121525009..121525212hg18UCSC Ensembl
Outerchr11:121519820..121527735hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg387916
hg197916
hg187916
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275465
Supporting Variants
Samples
Known GenesMIR100HG, MIRLET7A2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2586025
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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