A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013403



Internal ID19102621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152613523..152634908hg38UCSC Ensembl
Innerchr3:152331312..152352697hg19UCSC Ensembl
Innerchr3:153814002..153835387hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3821386
hg1921386
hg1821386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4922n100
Supporting Variantsnssv3606334
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)nsv1013403
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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