A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569198



Internal ID16009921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36871699..36903100hg38UCSC Ensembl
Innerchr15:37163900..37195301hg19UCSC Ensembl
Innerchr15:34951192..34982593hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3831402
hg1931402
hg1831402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840701
Samples
Known GenesLOC145845, MEIS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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