A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625503



Internal ID7012337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18572540..18577605hg38UCSC Ensembl
Innerchr11:18572690..18577455hg38UCSC Ensembl
Outerchr11:18572390..18577755hg38UCSC Ensembl
chr11:18594087..18599152hg19UCSC Ensembl
Innerchr11:18594237..18599002hg19UCSC Ensembl
Outerchr11:18593937..18599302hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385066
hg195066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14043307, essv14043308
SamplesHG00306, NA20868
Known GenesUEVLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625503
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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