A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4358n100



Internal ID20155974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10338676..10611996hg38UCSC Ensembl
chr21:10900461..11173781hg19UCSC Ensembl
chr21:9922332..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38273321
hg19273321
hg18273321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056642, nsv1064577, nsv1065506, nsv1057818, nsv1056842, nsv1066520, nsv1065471, nsv1063253
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)dgv4358n100
Frequency
Sample Size29084
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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