A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626731



Internal ID6666879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68034854..68035834hg38UCSC Ensembl
Innerchr11:68034925..68035564hg38UCSC Ensembl
Outerchr11:68034670..68036018hg38UCSC Ensembl
chr11:67802321..67803301hg19UCSC Ensembl
Innerchr11:67802392..67803031hg19UCSC Ensembl
Outerchr11:67802137..67803485hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14200058, essv14200062, essv14200057, essv14200059, essv14200060, essv14200063, essv14200056, essv14200061
SamplesHG01802, HG00599, HG02164, HG00560, HG00580, HG01866, HG01862, HG00728
Known GenesNDUFS8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626731
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer