A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5389n100



Internal ID22791476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:131487874..131539632hg38UCSC Ensembl
chr4:132409029..132460787hg19UCSC Ensembl
chr4:132628479..132680237hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3851759
hg1951759
hg1851759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031891, nsv1031060
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5389n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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