A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016404



Internal ID19105623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134142354..134154280hg38UCSC Ensembl
Innerchr8:135154597..135166523hg19UCSC Ensembl
Innerchr8:135223779..135235705hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3811927
hg1911927
hg1811927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692718
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)nsv1016404
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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