A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611409



Internal ID16398818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57525662..57630321hg38UCSC Ensembl
Innerchr8:58438221..58542880hg19UCSC Ensembl
Innerchr8:58600775..58705434hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38104660
hg19104660
hg18104660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12176n54
Supporting Variantsnssv1115602
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611409
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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