A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14174774



Internal ID4176590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59847853..59859203hg38UCSC Ensembl
Innerchr11:59847853..59859203hg38UCSC Ensembl
Outerchr11:59847542..59859486hg38UCSC Ensembl
chr11:59615326..59626676hg19UCSC Ensembl
Innerchr11:59615326..59626676hg19UCSC Ensembl
Outerchr11:59615015..59626959hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811351
hg1911351
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626542
Supporting Variants
SamplesNA18981
Known GenesTCN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14174774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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