A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521007



Internal ID18472602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95007177..95054932hg38UCSC Ensembl
Innerchr10:96766934..96814689hg19UCSC Ensembl
Innerchr10:96756924..96804679hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3847756
hg1947756
hg1847756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050544
Supporting Variants
Samples
Known GenesCYP2C8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521007
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