A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14220577



Internal ID1759372
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627046
Supporting Variants
SamplesHG01620
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14220577
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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