A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891930



Internal ID19186326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13061506..13094185hg38UCSC Ensembl
Outerchr11:13061506..13094185hg38UCSC Ensembl
Innerchr11:13083053..13115732hg19UCSC Ensembl
Outerchr11:13083053..13115732hg19UCSC Ensembl
Innerchr11:13039629..13072308hg18UCSC Ensembl
Outerchr11:13039629..13072308hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3832680
hg1932680
hg1832680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782522
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891930
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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