A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627598



Internal ID7014426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104856163..104889445hg38UCSC Ensembl
Innerchr11:104856163..104889445hg38UCSC Ensembl
Outerchr11:104855663..104889945hg38UCSC Ensembl
chr11:104726890..104760172hg19UCSC Ensembl
Innerchr11:104726890..104760172hg19UCSC Ensembl
Outerchr11:104726390..104760672hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3833283
hg1933283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14266242
SamplesNA18504
Known GenesCASP12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627598
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