A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626489



Internal ID7013321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56616817..56628020hg38UCSC Ensembl
Innerchr11:56616867..56627970hg38UCSC Ensembl
Outerchr11:56616715..56628122hg38UCSC Ensembl
chr11:56384293..56395496hg19UCSC Ensembl
Innerchr11:56384343..56395446hg19UCSC Ensembl
Outerchr11:56384191..56395598hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811204
hg1911204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14168335
SamplesNA20522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626489
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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