A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628141



Internal ID6668285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133089714..133090797hg38UCSC Ensembl
Innerchr11:133089714..133090797hg38UCSC Ensembl
Outerchr11:133089501..133091029hg38UCSC Ensembl
chr11:132959609..132960692hg19UCSC Ensembl
Innerchr11:132959609..132960692hg19UCSC Ensembl
Outerchr11:132959396..132960924hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14318162
SamplesNA19726
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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