A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569908



Internal ID16010631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71861659..71925695hg38UCSC Ensembl
Innerchr15:72154000..72218036hg19UCSC Ensembl
Innerchr15:69941054..70005090hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864037
hg1964037
hg1864037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4608n54
Supporting Variantsnssv844951, nssv844952
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569908
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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