A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751034



Internal ID12984586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84090927..84129229hg38UCSC Ensembl
Innerchr11:83801970..83840272hg19UCSC Ensembl
Innerchr11:83479618..83517920hg18UCSC Ensembl
Innerchr11:83479618..83517920hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3838303
hg1938303
hg1838303
hg1738303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6982218, essv6982217, essv6986108
SamplesBEC_404
Known GenesDLG2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751034
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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