A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627532



Internal ID7014360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102630296..102636418hg38UCSC Ensembl
chr11:102501027..102507149hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386123
hg196123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14254819, essv14254820
SamplesHG03603, HG01605
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627532
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