A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569237



Internal ID16009960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42125887..42145233hg38UCSC Ensembl
Innerchr15:42418085..42437431hg19UCSC Ensembl
Innerchr15:40205377..40224723hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3819347
hg1919347
hg1819347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842227
Samples
Known GenesPLA2G4F
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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