A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020831



Internal ID19110049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101371556..101401457hg38UCSC Ensembl
Innerchr8:102383784..102413685hg19UCSC Ensembl
Innerchr8:102452960..102482861hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3829902
hg1929902
hg1829902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689751
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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