A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589587



Internal ID18887868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32623361..32719438hg38UCSC Ensembl
Innerchr3:32664853..32760930hg19UCSC Ensembl
Innerchr3:32639857..32735934hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3896078
hg1996078
hg1896078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004530
Supporting Variants
Samples
Known GenesCNOT10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589587
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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