A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7910n54



Internal ID22775805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45968237..45978497hg38UCSC Ensembl
chr21:47388151..47398411hg19UCSC Ensembl
chr21:46212579..46222839hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810261
hg1910261
hg1810261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587883, nsv587929
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7910n54
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