A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611097



Internal ID16398506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40324784..40331544hg38UCSC Ensembl
Innerchr8:40182303..40189063hg19UCSC Ensembl
Innerchr8:40301460..40308220hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg386761
hg196761
hg186761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12114n54
Supporting Variantsnssv1111270
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611097
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