A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589509



Internal ID18887790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25543343..25570244hg38UCSC Ensembl
Innerchr3:25584834..25611735hg19UCSC Ensembl
Innerchr3:25559838..25586739hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3826902
hg1926902
hg1826902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004065
Supporting Variants
Samples
Known GenesRARB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589509
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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