A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14243438



Internal ID3821522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95276821..95280638hg38UCSC Ensembl
Innerchr11:95276845..95280615hg38UCSC Ensembl
Outerchr11:95276798..95280662hg38UCSC Ensembl
chr11:95009985..95013802hg19UCSC Ensembl
Innerchr11:95010009..95013779hg19UCSC Ensembl
Outerchr11:95009962..95013826hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383818
hg193818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627343
Supporting Variants
SamplesHG03460
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14243438
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