A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892044



Internal ID19186440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84763874..84850255hg38UCSC Ensembl
Outerchr11:84763874..84850255hg38UCSC Ensembl
Innerchr11:84474917..84561299hg19UCSC Ensembl
Outerchr11:84474917..84561299hg19UCSC Ensembl
Innerchr11:84152565..84238947hg18UCSC Ensembl
Outerchr11:84152565..84238947hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3886382
hg1986383
hg1886383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779640
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892044
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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