A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004891



Internal ID19094108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89355938..89371326hg38UCSC Ensembl
Innerchr3:89405088..89420476hg19UCSC Ensembl
Innerchr3:89487778..89503166hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3815389
hg1915389
hg1815389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4808n100
Supporting Variantsnssv3735141
Samples
Known GenesEPHA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004891
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