A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4182n54



Internal ID22772077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20300975..21165865hg38UCSC Ensembl
chr15:20506228..21371194hg19UCSC Ensembl
chr15:18766242..19635853hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38864891
hg19864967
hg18869612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567448, nsv567429, nsv567461, nsv567340, nsv567350, nsv567403, nsv567390, nsv567441, nsv567459, nsv567328, nsv567319, nsv567351
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4182n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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