A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6060807



Internal ID8843265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84099928..84101762hg38UCSC Ensembl
Outerchr11:84099891..84101812hg38UCSC Ensembl
Innerchr11:83810971..83812805hg19UCSC Ensembl
Outerchr11:83810934..83812855hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381922
hg191922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661588
Supporting Variants
SamplesHG00280
Known GenesDLG2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6060807
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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