A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627046



Internal ID7013876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84424759..84484960hg38UCSC Ensembl
Innerchr11:84424759..84484960hg38UCSC Ensembl
Outerchr11:84424259..84485460hg38UCSC Ensembl
chr11:84135802..84196003hg19UCSC Ensembl
Innerchr11:84135802..84196003hg19UCSC Ensembl
Outerchr11:84135302..84196503hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3860202
hg1960202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14220578, essv14220577
SamplesNA21115, HG01620
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627046
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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