A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4731n100



Internal ID20156347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46733893..46827326hg38UCSC Ensembl
chr3:46775383..46868816hg19UCSC Ensembl
chr3:46750387..46843820hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3893434
hg1993434
hg1893434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999980, nsv998699
Samples
Known GenesPRSS45, PRSS46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4731n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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