A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7825n54



Internal ID22775720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34888828..34889994hg38UCSC Ensembl
chr21:36261125..36262291hg19UCSC Ensembl
chr21:35182995..35184161hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg381167
hg191167
hg181167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587432, nsv587443
Samples
Known GenesRUNX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7825n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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