A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4808n100



Internal ID22790895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89355938..89371326hg38UCSC Ensembl
chr3:89405088..89420476hg19UCSC Ensembl
chr3:89487778..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 Variants
Supporting Variantsnsv1007458, nsv1004891, nsv999984, nsv1000972, nsv1008373, nsv1009652, nsv1012294, nsv1011887, nsv1012186, nsv1014536, nsv1008556, nsv1001172, nsv1002861, nsv1008481, nsv1007795, nsv1010705, nsv1000450, nsv1007058, nsv1010377, nsv1009969, nsv1014665, nsv1002355
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)dgv4808n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss125
Observed Complex0
Frequencyn/a


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