A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625387



Internal ID7012221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12070135..12075168hg38UCSC Ensembl
Innerchr11:12070185..12075118hg38UCSC Ensembl
Outerchr11:12070085..12075218hg38UCSC Ensembl
chr11:12091682..12096715hg19UCSC Ensembl
Innerchr11:12091732..12096665hg19UCSC Ensembl
Outerchr11:12091632..12096765hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14031726, essv14031727, essv14031728
SamplesHG03738, HG03837, HG03644
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625387
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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