A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008836



Internal ID19098054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45203611..45248515hg38UCSC Ensembl
Innerchr3:45245103..45290007hg19UCSC Ensembl
Innerchr3:45220107..45265011hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844905
hg1944905
hg1844905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589737
Samples
Known GenesTMEM158
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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