A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4610n54



Internal ID20138034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71969044..72015350hg38UCSC Ensembl
chr15:72261385..72307691hg19UCSC Ensembl
chr15:70048439..70094745hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3846307
hg1946307
hg1846307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569915, nsv569913
SamplesNINDS_222
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4610n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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