A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017110



Internal ID18759645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25147550..25210253hg38UCSC Ensembl
Innerchr8:25005065..25067769hg19UCSC Ensembl
Innerchr8:25060982..25123686hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3862704
hg1962705
hg1862705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685494
Samples
Known GenesDOCK5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017110
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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