A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2244n100



Internal ID22788331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20327352..20681492hg38UCSC Ensembl
chr15:20532605..20886821hg19UCSC Ensembl
chr15:18792619..19146835hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38354141
hg19354217
hg18354217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044322, nsv1054308, nsv1054887, nsv1047598, nsv1037040, nsv1036154, nsv1047115, nsv1053484, nsv1053944, nsv1046484, nsv1039341, nsv1049793, nsv1044935, nsv1036433, nsv1040648, nsv1044492, nsv1038240, nsv1054123, nsv1045603, nsv1044431, nsv1043199, nsv1038531, nsv1054559, nsv1050332
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2244n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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