A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013893



Internal ID19103112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89331991..89370219hg38UCSC Ensembl
Innerchr3:89381141..89419369hg19UCSC Ensembl
Innerchr3:89463831..89502059hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3838229
hg1938229
hg1838229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596287
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)nsv1013893
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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