A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14211153



Internal ID5373882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72532439..72536943hg38UCSC Ensembl
Innerchr11:72532439..72536943hg38UCSC Ensembl
Outerchr11:72532274..72537148hg38UCSC Ensembl
chr11:72243483..72247987hg19UCSC Ensembl
Innerchr11:72243483..72247987hg19UCSC Ensembl
Outerchr11:72243318..72248192hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384505
hg194505
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626803
Supporting Variants
SamplesNA18916
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14211153
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