A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14073375



Internal ID4653187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28373563..28387486hg38UCSC Ensembl
Innerchr11:28374063..28386986hg38UCSC Ensembl
Outerchr11:28372563..28388486hg38UCSC Ensembl
chr11:28395110..28409033hg19UCSC Ensembl
Innerchr11:28395610..28408533hg19UCSC Ensembl
Outerchr11:28394110..28410033hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3813924
hg1913924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625783
Supporting Variants
SamplesHG04183
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14073375
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