A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4363n54



Internal ID22772258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24214032..24524321hg38UCSC Ensembl
chr15:24459179..24769468hg19UCSC Ensembl
chr15:22010272..22320561hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38310290
hg19310290
hg18310290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568472, nsv568464, nsv568468, nsv568465
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4363n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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