A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2213n100



Internal ID22788300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20190264..22095238hg38UCSC Ensembl
chr15:20395517..22383189hg19UCSC Ensembl
chr15:18655531..19884553hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381904975
hg191987673
hg181229023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048832, nsv1041499, nsv1039135, nsv1039771, nsv1047106, nsv1054163, nsv1048267, nsv1052368, nsv1037254, nsv1050483, nsv1042561, nsv1054396, nsv1046977, nsv1036413, nsv1055075, nsv1041815, nsv1044164, nsv1047960, nsv1049110, nsv1054315, nsv1036568, nsv1054340, nsv1047316, nsv1052373, nsv1037071, nsv1039397, nsv1043858, nsv1048903, nsv1036257, nsv1042852, nsv1049562, nsv1038136, nsv1054886
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2213n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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