A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7827n54



Internal ID22775722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34888828..34890332hg38UCSC Ensembl
chr21:36261125..36262629hg19UCSC Ensembl
chr21:35182995..35184499hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg381505
hg191505
hg181505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587438, nsv587434, nsv587445, nsv587435, nsv587444
Samples
Known GenesRUNX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7827n54
Frequency
Sample Size17421
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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