A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891942



Internal ID19186338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20978012..21000461hg38UCSC Ensembl
Outerchr11:20978012..21000461hg38UCSC Ensembl
Innerchr11:20999558..21022007hg19UCSC Ensembl
Outerchr11:20999558..21022007hg19UCSC Ensembl
Innerchr11:20956134..20978583hg18UCSC Ensembl
Outerchr11:20956134..20978583hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822450
hg1922450
hg1822450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797660
Samples
Known GenesNELL1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891942
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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