A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002258



Internal ID19091475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:78432819..78483028hg38UCSC Ensembl
Innerchr3:78481969..78532178hg19UCSC Ensembl
Innerchr3:78564659..78614868hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3850210
hg1950210
hg1850210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596225
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)nsv1002258
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