A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627048



Internal ID7013878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84478094..84517378hg38UCSC Ensembl
Innerchr11:84478094..84517378hg38UCSC Ensembl
Outerchr11:84477594..84517878hg38UCSC Ensembl
chr11:84189137..84228421hg19UCSC Ensembl
Innerchr11:84189137..84228421hg19UCSC Ensembl
Outerchr11:84188637..84228921hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3839285
hg1939285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14220582, essv14220583
SamplesNA21115, HG01620
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627048
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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