A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569915



Internal ID16010638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71974823..72015350hg38UCSC Ensembl
Innerchr15:72267164..72307691hg19UCSC Ensembl
Innerchr15:70054218..70094745hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3840528
hg1940528
hg1840528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4610n54
Supporting Variantsnssv844956
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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