A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569906



Internal ID16010629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71833693..71925695hg38UCSC Ensembl
Innerchr15:72126034..72218036hg19UCSC Ensembl
Innerchr15:69913088..70005090hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3892003
hg1992003
hg1892003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844949
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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