A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593095



Internal ID18544690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17131923..17166775hg38UCSC Ensembl
Innerchr3:17173415..17208267hg19UCSC Ensembl
Innerchr3:17148419..17183271hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3834853
hg1934853
hg1834853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008636
Supporting Variants
Samples
Known GenesTBC1D5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593095
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