A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891963



Internal ID18839673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34445990..34451874hg38UCSC Ensembl
Outerchr11:34445990..34451874hg38UCSC Ensembl
Innerchr11:34467537..34473421hg19UCSC Ensembl
Outerchr11:34467537..34473421hg19UCSC Ensembl
Innerchr11:34424113..34429997hg18UCSC Ensembl
Outerchr11:34424113..34429997hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385885
hg195885
hg185885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797154
Samples
Known GenesCAT
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891963
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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