A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7893n54



Internal ID20141317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44886246..44902938hg38UCSC Ensembl
chr21:46306161..46322853hg19UCSC Ensembl
chr21:45130589..45147281hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816693
hg1916693
hg1816693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587816, nsv587815
SamplesHGDP00676
Known GenesITGB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7893n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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