A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012569



Internal ID19101786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42317382..42331147hg38UCSC Ensembl
Innerchr3:42358874..42372639hg19UCSC Ensembl
Innerchr3:42333878..42347643hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3813766
hg1913766
hg1813766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4727n100
Supporting Variantsnssv3589727, nssv3589723, nssv3589721, nssv3589724, nssv3589725, nssv3589722, nssv3589726
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)nsv1012569
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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