A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705343



Internal ID15095309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61690385..61919561hg38UCSC Ensembl
Innerchr11:61457857..61687033hg19UCSC Ensembl
Innerchr11:61214433..61443609hg18UCSC Ensembl
Innerchr11:61214433..61443609hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38229177
hg19229177
hg18229177
hg17229177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528697
Supporting Variants
Samples
Known GenesDAGLA, DKFZP434K028, FADS1, FADS2, FADS3, FEN1, MIR1908, MIR611, MIR6746, MYRF, RAB3IL1, TMEM258
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705343
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer