A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4612n54



Internal ID20138036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72093834..72095338hg38UCSC Ensembl
chr15:72386175..72387679hg19UCSC Ensembl
chr15:70173229..70174733hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381505
hg191505
hg181505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569920, nsv569921
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4612n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer