A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891953



Internal ID19186349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25448144..26061883hg38UCSC Ensembl
Outerchr11:25448144..26061883hg38UCSC Ensembl
Innerchr11:25469690..26083430hg19UCSC Ensembl
Outerchr11:25469690..26083430hg19UCSC Ensembl
Innerchr11:25426266..26040006hg18UCSC Ensembl
Outerchr11:25426266..26040006hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38613740
hg19613741
hg18613741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800620
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891953
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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