A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4786n54



Internal ID22772681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100879403..100880220hg38UCSC Ensembl
chr15:101419608..101420425hg19UCSC Ensembl
chr15:99237131..99237948hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38818
hg19818
hg18818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570821, nsv570818, nsv570819, nsv570824
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4786n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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