A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14293213



Internal ID2119832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118737005..118745922hg38UCSC Ensembl
Innerchr11:118737065..118745863hg38UCSC Ensembl
Outerchr11:118736946..118745982hg38UCSC Ensembl
chr11:118607714..118616631hg19UCSC Ensembl
Innerchr11:118607774..118616572hg19UCSC Ensembl
Outerchr11:118607655..118616691hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388918
hg198918
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627877
Supporting Variants
SamplesHG01924
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14293213
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