A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6218545



Internal ID9761654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95540542..95552092hg38UCSC Ensembl
Outerchr11:95540505..95552142hg38UCSC Ensembl
Innerchr11:95273706..95285256hg19UCSC Ensembl
Outerchr11:95273669..95285306hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811638
hg1911638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656726
Supporting Variants
SamplesNA19717
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6218545
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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