A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999384



Internal ID18812234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24483854..24615382hg38UCSC Ensembl
Innerchr3:24525345..24656873hg19UCSC Ensembl
Innerchr3:24500349..24631877hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38131529
hg19131529
hg18131529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589500
Samples
Known GenesMIR4792, THRB, THRB-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999384
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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