A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512406



Internal ID15505145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72093165..72095843hg38UCSC Ensembl
Outerchr15:72385506..72388184hg19UCSC Ensembl
Outerchr15:70172560..70175238hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382679
hg192679
hg182679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624996
Samples1
Known GenesMYO9A
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512406
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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