A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002786



Internal ID19092003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99225602..99295092hg38UCSC Ensembl
Innerchr3:98944446..99013936hg19UCSC Ensembl
Innerchr3:100427136..100496626hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3869491
hg1969491
hg1869491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4828n100
Supporting Variantsnssv3604229
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)nsv1002786
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