A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv177e214



Internal ID22756071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3925680..3951521hg38UCSC Ensembl
chr11:3946910..3972751hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825842
hg1925842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3625160, esv3625159
SamplesNA18638, HG02805
Known GenesSTIM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv177e214
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