A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569917



Internal ID16010640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71992306..72037565hg38UCSC Ensembl
Innerchr15:72284647..72329906hg19UCSC Ensembl
Innerchr15:70071701..70116960hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3845260
hg1945260
hg1845260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149601
SamplesHGDP01355
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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