A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7743n54



Internal ID20141167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10324453..10728641hg38UCSC Ensembl
chr21:10783816..11188004hg19UCSC Ensembl
chr21:9805687..10209875hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38404189
hg19404189
hg18404189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586948, nsv586972
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7743n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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