A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611226



Internal ID16398635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45930514..45975113hg38UCSC Ensembl
Innerchr8:46842136..46886735hg19UCSC Ensembl
Innerchr8:46961301..47005900hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3844600
hg1944600
hg1844600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1114116
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611226
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