A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14009027



Internal ID3801765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6168439..6171798hg38UCSC Ensembl
Innerchr11:6168443..6171794hg38UCSC Ensembl
Outerchr11:6168435..6171802hg38UCSC Ensembl
chr11:6189669..6193028hg19UCSC Ensembl
Innerchr11:6189673..6193024hg19UCSC Ensembl
Outerchr11:6189665..6193032hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625262
Supporting Variants
SamplesHG03446
Known GenesOR52B2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14009027
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