A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625476



Internal ID7012310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17382108..17384528hg38UCSC Ensembl
Innerchr11:17382125..17384511hg38UCSC Ensembl
Outerchr11:17382091..17384545hg38UCSC Ensembl
chr11:17403655..17406075hg19UCSC Ensembl
Innerchr11:17403672..17406058hg19UCSC Ensembl
Outerchr11:17403638..17406092hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14040157, essv14040158
SamplesHG04185, HG04227
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625476
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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