A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065416



Internal ID19154635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14108872..14167302hg38UCSC Ensembl
Innerchr17:14012189..14070619hg19UCSC Ensembl
Innerchr17:13952914..14011344hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3858431
hg1958431
hg1858431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560363
Samples
Known GenesCOX10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065416
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