A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2211n100



Internal ID22788298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20190264..20952464hg38UCSC Ensembl
chr15:20395517..21157793hg19UCSC Ensembl
chr15:18655531..19422452hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38762201
hg19762277
hg18766922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038237, nsv1048284, nsv1037180, nsv1049307, nsv1049794, nsv1041020, nsv1035225, nsv1053770, nsv1049109
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)dgv2211n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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