A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569912



Internal ID16010635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71911176..72033254hg38UCSC Ensembl
Innerchr15:72203517..72325595hg19UCSC Ensembl
Innerchr15:69990571..70112649hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38122079
hg19122079
hg18122079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4609n54
Supporting Variantsnssv844955
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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