A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7834n54



Internal ID20141258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41369022..41395967hg38UCSC Ensembl
chr21:42740949..42767894hg19UCSC Ensembl
chr21:41662819..41689764hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826946
hg1926946
hg1826946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587494, nsv587495
Samples
Known GenesMX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7834n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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