A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14232113



Internal ID5069089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90674566..90682328hg38UCSC Ensembl
Innerchr11:90674617..90682277hg38UCSC Ensembl
Outerchr11:90674515..90682379hg38UCSC Ensembl
chr11:90407734..90415496hg19UCSC Ensembl
Innerchr11:90407785..90415445hg19UCSC Ensembl
Outerchr11:90407683..90415547hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg387763
hg197763
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627216
Supporting Variants
SamplesNA18539
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14232113
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer