A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4368n100



Internal ID20155984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10338676..10558343hg38UCSC Ensembl
chr21:10954114..11173781hg19UCSC Ensembl
chr21:9975985..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38219668
hg19219668
hg18219668
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063631, nsv1065874, nsv1065404
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4368n100
Frequency
Sample Size29084
Observed Gain18
Observed Loss3
Observed Complex0
Frequencyn/a


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