A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4783n54



Internal ID20138207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100879147..100880322hg38UCSC Ensembl
chr15:101419352..101420527hg19UCSC Ensembl
chr15:99236875..99238050hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381176
hg191176
hg181176
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570811, nsv570809, nsv570813, nsv570814
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4783n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss8
Observed Complex0
Frequencyn/a


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