A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569907



Internal ID16010630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71861659..71922724hg38UCSC Ensembl
Innerchr15:72154000..72215065hg19UCSC Ensembl
Innerchr15:69941054..70002119hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861066
hg1961066
hg1861066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4608n54
Supporting Variantsnssv844950
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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