A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625122



Internal ID7011960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2124001..2125669hg38UCSC Ensembl
Innerchr11:2124009..2125661hg38UCSC Ensembl
Outerchr11:2123993..2125677hg38UCSC Ensembl
chr11:2145231..2146899hg19UCSC Ensembl
Innerchr11:2145239..2146891hg19UCSC Ensembl
Outerchr11:2145223..2146907hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993597
SamplesHG03727
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625122
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