A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627908



Internal ID7014733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120709549..120712893hg38UCSC Ensembl
Innerchr11:120709553..120712890hg38UCSC Ensembl
Outerchr11:120709546..120712897hg38UCSC Ensembl
chr11:120580258..120583602hg19UCSC Ensembl
Innerchr11:120580262..120583599hg19UCSC Ensembl
Outerchr11:120580255..120583606hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383345
hg193345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14295208, essv14295209
SamplesHG00306, HG03775
Known GenesGRIK4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627908
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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