A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4523n54



Internal ID20137947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49253235..49255076hg38UCSC Ensembl
chr15:49545432..49547273hg19UCSC Ensembl
chr15:47332724..47334565hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381842
hg191842
hg181842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569376, nsv569382, nsv569379
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4523n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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