A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627331



Internal ID7014161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94885473..94890397hg38UCSC Ensembl
Innerchr11:94885973..94889897hg38UCSC Ensembl
Outerchr11:94884473..94891397hg38UCSC Ensembl
chr11:94618638..94623562hg19UCSC Ensembl
Innerchr11:94619138..94623062hg19UCSC Ensembl
Outerchr11:94617638..94624562hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384925
hg194925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv223e214
Supporting Variantsessv14241871
SamplesHG03696
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627331
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