A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8242n54



Internal ID22776137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16197487..16199512hg38UCSC Ensembl
chr3:16238994..16241019hg19UCSC Ensembl
chr3:16213998..16216023hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382026
hg192026
hg182026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589816, nsv589815
Samples
Known GenesGALNT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8242n54
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