A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14168335



Internal ID6476441
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626489
Supporting Variants
SamplesNA20522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14168335
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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