A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611312



Internal ID16398721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:50017515..50098562hg38UCSC Ensembl
Innerchr8:50930075..51011122hg19UCSC Ensembl
Innerchr8:51092628..51173675hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3881048
hg1981048
hg1881048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115123
Samples
Known GenesSNTG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611312
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