A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4174n54



Internal ID22772069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20051457..20762254hg38UCSC Ensembl
chr15:20256710..20967583hg19UCSC Ensembl
chr15:18516724..19227614hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38710798
hg19710874
hg18710891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567199, nsv567189
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4174n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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