A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570387



Internal ID16011110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89677442..89692000hg38UCSC Ensembl
Innerchr15:90220673..90235231hg19UCSC Ensembl
Innerchr15:88021677..88036235hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814559
hg1914559
hg1814559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848200
Samples
Known GenesPEX11A, PLIN1, WDR93
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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