A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6190960



Internal ID9154243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79631580..79637943hg38UCSC Ensembl
Outerchr11:79631543..79637993hg38UCSC Ensembl
Innerchr11:79342624..79348987hg19UCSC Ensembl
Outerchr11:79342587..79349037hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386451
hg196451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661272
Supporting Variants
SamplesHG01350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6190960
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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