A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2195n100



Internal ID22788282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20011690..20828285hg38UCSC Ensembl
chr15:20216943..21033614hg19UCSC Ensembl
chr15:18476957..19296118hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38816596
hg19816672
hg18819162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046494, nsv1052819, nsv1054983, nsv1044468, nsv1042482, nsv1043451, nsv1054216, nsv1052358, nsv1043783, nsv1039427, nsv1038699, nsv1052164, nsv1047589
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2195n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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