A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611235



Internal ID16398644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46149355..46828229hg38UCSC Ensembl
Innerchr8:47060977..47739851hg19UCSC Ensembl
Innerchr8:47180142..47859016hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38678875
hg19678875
hg18678875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156610
Samples1787431197_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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