A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628079



Internal ID7014904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130249132..130250580hg38UCSC Ensembl
Innerchr11:130249169..130250544hg38UCSC Ensembl
Outerchr11:130249096..130250617hg38UCSC Ensembl
chr11:130119027..130120475hg19UCSC Ensembl
Innerchr11:130119064..130120439hg19UCSC Ensembl
Outerchr11:130118991..130120512hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14312321
SamplesNA20520
Known GenesZBTB44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628079
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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