A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569918



Internal ID16010641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72090888..72095726hg38UCSC Ensembl
Innerchr15:72383229..72388067hg19UCSC Ensembl
Innerchr15:70170283..70175121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384839
hg194839
hg184839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844958, nssv844959
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569918
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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