A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5682414



Internal ID8659817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62493688..62494961hg38UCSC Ensembl
Outerchr11:62493531..62495160hg38UCSC Ensembl
Innerchr11:62261160..62262433hg19UCSC Ensembl
Outerchr11:62261003..62262632hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674790
Supporting Variants
SamplesNA19107
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5682414
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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