A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14159423



Internal ID4161239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55287669..55568298hg38UCSC Ensembl
Innerchr11:55287694..55568274hg38UCSC Ensembl
Outerchr11:55287645..55568323hg38UCSC Ensembl
chr11:55055145..55335774hg19UCSC Ensembl
Innerchr11:55055170..55335750hg19UCSC Ensembl
Outerchr11:55055121..55335799hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38280630
hg19280630
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626425
Supporting Variants
SamplesHG00599
Known GenesOR4A15, OR4A16, OR4C15, TRIM51HP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14159423
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