A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026296



Internal ID19115513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..261945hg38UCSC Ensembl
Innerchr9:46587..261945hg19UCSC Ensembl
Innerchr9:36587..251945hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38215359
hg19215359
hg18215359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7344n100
Supporting Variantsnssv3690942
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026296
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