A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011402



Internal ID19100619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89334971..89395845hg38UCSC Ensembl
Innerchr3:89384121..89444995hg19UCSC Ensembl
Innerchr3:89466811..89527685hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3860875
hg1960875
hg1860875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4804n100
Supporting Variantsnssv3596289
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)nsv1011402
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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