A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2332n100



Internal ID22788419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20802132..22236602hg38UCSC Ensembl
chr15:21007461..22524553hg19UCSC Ensembl
chr15:19267484..20025917hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381434471
hg191517093
hg18758434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036782, nsv1041472, nsv1043147, nsv1036624, nsv1046011, nsv1050257, nsv1047167, nsv1038784, nsv1047059, nsv1054230, nsv1037108
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, 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)dgv2332n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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