A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030923



Internal ID19120143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72380391..72510979hg38UCSC Ensembl
Innerchr8:73292626..73423214hg19UCSC Ensembl
Innerchr8:73455180..73585768hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38130589
hg19130589
hg18130589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689528
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)nsv1030923
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