A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625551



Internal ID7012385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20119264..20120433hg38UCSC Ensembl
Innerchr11:20119291..20120407hg38UCSC Ensembl
Outerchr11:20119238..20120460hg38UCSC Ensembl
chr11:20140810..20141979hg19UCSC Ensembl
Innerchr11:20140837..20141953hg19UCSC Ensembl
Outerchr11:20140784..20142006hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14047177
SamplesHG01746
Known GenesNAV2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625551
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