A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628125



Internal ID6668269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132423818..132426870hg38UCSC Ensembl
Innerchr11:132423818..132426870hg38UCSC Ensembl
Outerchr11:132423318..132427370hg38UCSC Ensembl
chr11:132293712..132296764hg19UCSC Ensembl
Innerchr11:132293712..132296764hg19UCSC Ensembl
Outerchr11:132293212..132297264hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383053
hg193053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317600
SamplesHG02116
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628125
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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