A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611131



Internal ID16398540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42331225..42336565hg38UCSC Ensembl
Innerchr8:42188743..42194083hg19UCSC Ensembl
Innerchr8:42307900..42313240hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385341
hg195341
hg185341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1112243
Samples
Known GenesIKBKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611131
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