A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009111



Internal ID19098329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166860342..166932651hg38UCSC Ensembl
Innerchr3:166578130..166650439hg19UCSC Ensembl
Innerchr3:168060824..168133133hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3872310
hg1972310
hg1872310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612695
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)nsv1009111
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