A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999448



Internal ID19158985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65213280..65230894hg38UCSC Ensembl
Innerchr3:65198955..65216569hg19UCSC Ensembl
Innerchr3:65173995..65191609hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3817615
hg1917615
hg1817615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4768n100
Supporting Variantsnssv3593952
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)nsv999448
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