A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6154226



Internal ID9539988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91760440..91764401hg38UCSC Ensembl
Outerchr11:91760283..91764554hg38UCSC Ensembl
Innerchr11:91493606..91497567hg19UCSC Ensembl
Outerchr11:91493449..91497720hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384272
hg194272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667395
Supporting Variants
SamplesNA19070
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6154226
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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