A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569941



Internal ID16010664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094765..72095726hg38UCSC Ensembl
Innerchr15:72387106..72388067hg19UCSC Ensembl
Innerchr15:70174160..70175121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38962
hg19962
hg18962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4615n54
Supporting Variantsnssv845074, nssv845071, nssv845073, nssv845072
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569941
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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