A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088549



Internal ID1023159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33993272..33996502hg38UCSC Ensembl
Innerchr11:33993273..33996502hg38UCSC Ensembl
Outerchr11:33993272..33996503hg38UCSC Ensembl
chr11:34014819..34018049hg19UCSC Ensembl
Innerchr11:34014820..34018049hg19UCSC Ensembl
Outerchr11:34014819..34018050hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383231
hg193231
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625902
Supporting Variants
SamplesHG00640
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088549
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