A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7734n54



Internal ID22775629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10560297..10754646hg38UCSC Ensembl
chr21:10757811..10952160hg19UCSC Ensembl
chr21:9779682..9974031hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38194350
hg19194350
hg18194350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586909, nsv586908, nsv586907
Samples
Known GenesTPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7734n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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