A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569931



Internal ID16010654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094085..72095477hg38UCSC Ensembl
Innerchr15:72386426..72387818hg19UCSC Ensembl
Innerchr15:70173480..70174872hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381393
hg191393
hg181393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4614n54
Supporting Variantsnssv845051
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569931
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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