A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2210n100



Internal ID22788297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20190264..20890462hg38UCSC Ensembl
chr15:20395517..21095791hg19UCSC Ensembl
chr15:18655531..19360450hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38700199
hg19700275
hg18704920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044249, nsv1052969, nsv1036306, nsv1046346, nsv1046721, nsv1046553, nsv1050979, nsv1038783, nsv1044144, nsv1051608
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)dgv2210n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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