A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14301926



Internal ID6345585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124357109..124358989hg38UCSC Ensembl
Innerchr11:124357149..124358949hg38UCSC Ensembl
Outerchr11:124357069..124359029hg38UCSC Ensembl
chr11:124227005..124228885hg19UCSC Ensembl
Innerchr11:124227045..124228845hg19UCSC Ensembl
Outerchr11:124226965..124228925hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627977
Supporting Variants
SamplesNA20274
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14301926
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