A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4769n54



Internal ID20138193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99700705..100224933hg38UCSC Ensembl
chr15:100240910..100765138hg19UCSC Ensembl
chr15:98058433..98582661hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38524229
hg19524229
hg18524229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570732, nsv570730, nsv570734
SamplesHGDP00684, HGDP00686
Known GenesADAMTS17, DNM1P46, LYSMD4, MEF2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4769n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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