A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7849n54



Internal ID19000025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41863326..41898934hg38UCSC Ensembl
chr21:43283435..43319043hg19UCSC Ensembl
chr21:42156504..42192112hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3835609
hg1935609
hg1835609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587566, nsv587567
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7849n54
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