A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7977n54



Internal ID22775872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18913491..19020595hg38UCSC Ensembl
chr22:18901004..19008108hg19UCSC Ensembl
chr22:17281004..17388108hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38107105
hg19107105
hg18107105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588206, nsv588199
SamplesHGDP01042
Known GenesDGCR5, DGCR9, PRODH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7977n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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