A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2789n100



Internal ID22788876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19928432..19956028hg38UCSC Ensembl
chr16:19939754..19967350hg19UCSC Ensembl
chr16:19847255..19874851hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3827597
hg1927597
hg1827597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046734, nsv1053734, nsv1048434, nsv1037239, nsv1046426, nsv1047656, nsv1045359, nsv1052032, nsv1045580, nsv1047130, nsv1048331, nsv1048219, nsv1053926, nsv1052157, nsv1036514, nsv1040489, nsv1046555, nsv1049727, nsv1051598, nsv1035253, nsv1045258, nsv1046500, nsv1043040, nsv1038148, nsv1050513
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)dgv2789n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss1853
Observed Complex0
Frequencyn/a


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