A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008123



Internal ID19097342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140609983..140745944hg38UCSC Ensembl
Innerchr3:140328825..140464786hg19UCSC Ensembl
Innerchr3:141811515..141947476hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38135962
hg19135962
hg18135962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4911n100
Supporting Variantsnssv3606100
Samples
Known GenesTRIM42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008123
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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