A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008373



Internal ID19097591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89356604..89370759hg38UCSC Ensembl
Innerchr3:89405754..89419909hg19UCSC Ensembl
Innerchr3:89488444..89502599hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3814156
hg1914156
hg1814156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4808n100
Supporting Variantsnssv3603199
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)nsv1008373
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