A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891923



Internal ID19186319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6154881..6183086hg38UCSC Ensembl
Outerchr11:6154881..6183086hg38UCSC Ensembl
Innerchr11:6176111..6204316hg19UCSC Ensembl
Outerchr11:6176111..6204316hg19UCSC Ensembl
Innerchr11:6132687..6160892hg18UCSC Ensembl
Outerchr11:6132687..6160892hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828206
hg1928206
hg1828206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796747
Samples
Known GenesOR52B2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891923
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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