A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626547



Internal ID6666697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60084926..60104676hg38UCSC Ensembl
Innerchr11:60085426..60104176hg38UCSC Ensembl
Outerchr11:60083926..60105676hg38UCSC Ensembl
chr11:59852399..59872149hg19UCSC Ensembl
Innerchr11:59852899..59871649hg19UCSC Ensembl
Outerchr11:59851399..59873149hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3819751
hg1919751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv201e214
Supporting Variantsessv14174898
SamplesHG03786
Known GenesMS4A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626547
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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