A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589550



Internal ID18887831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26491082..26579428hg38UCSC Ensembl
Innerchr3:26532573..26620919hg19UCSC Ensembl
Innerchr3:26507577..26595923hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3888347
hg1988347
hg1888347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008907
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)nssv3589550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer