A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589485



Internal ID18887766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22512780..22992007hg38UCSC Ensembl
Innerchr3:22554271..23033498hg19UCSC Ensembl
Innerchr3:22529275..23008502hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38479228
hg19479228
hg18479228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014828
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589485
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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