A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611841



Internal ID16399250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106035831..106078272hg38UCSC Ensembl
Innerchr8:107048059..107090500hg19UCSC Ensembl
Innerchr8:107117235..107159676hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3842442
hg1942442
hg1842442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118236
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611841
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