A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660409



Internal ID9926514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134134088..134138032hg38UCSC Ensembl
Outerchr11:134133931..134138185hg38UCSC Ensembl
Innerchr11:134003983..134007927hg19UCSC Ensembl
Outerchr11:134003826..134008080hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384255
hg194255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5434410, essv6381130
SamplesHG00701, NA18548
Known GenesJAM3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660409
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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