A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008636



Internal ID18751167
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 StatusM
Merged Variants
Supporting Variantsnssv3593095
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)nsv1008636
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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