A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569925



Internal ID16010648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72094765hg38UCSC Ensembl
Innerchr15:72386349..72387106hg19UCSC Ensembl
Innerchr15:70173403..70174160hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38758
hg19758
hg18758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844992, nssv844991, nssv844994, nssv844993
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569925
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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