A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7875n54



Internal ID19000051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43739631..43740914hg38UCSC Ensembl
chr21:45159512..45160795hg19UCSC Ensembl
chr21:43983940..43985223hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381284
hg191284
hg181284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587705, nsv587710, nsv587706, nsv587707
Samples
Known GenesPDXK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7875n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer