A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569939



Internal ID16010662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094294..72095450hg38UCSC Ensembl
Innerchr15:72386635..72387791hg19UCSC Ensembl
Innerchr15:70173689..70174845hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381157
hg191157
hg181157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4614n54
Supporting Variantsnssv845069
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569939
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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