A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6381130



Internal ID9352630
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 Flag1
Merged StatusS
Merged Variantsesv2660409
Supporting Variants
SamplesNA18548
Known GenesJAM3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6381130
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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