A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14286887



Internal ID4288703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111289595..111291946hg38UCSC Ensembl
Innerchr11:111289595..111291946hg38UCSC Ensembl
Outerchr11:111289343..111292287hg38UCSC Ensembl
chr11:111160320..111162671hg19UCSC Ensembl
Innerchr11:111160320..111162671hg19UCSC Ensembl
Outerchr11:111160068..111163012hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627730
Supporting Variants
SamplesNA18623
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14286887
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