A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4770n54



Internal ID22772665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99789846..100059028hg38UCSC Ensembl
chr15:100330051..100599233hg19UCSC Ensembl
chr15:98147574..98416756hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38269183
hg19269183
hg18269183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570733, nsv570731
SamplesHGDP00986, HGDP01094
Known GenesADAMTS17, DNM1P46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4770n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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