A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569336



Internal ID16356745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48060055..48111670hg38UCSC Ensembl
Innerchr15:48352252..48403867hg19UCSC Ensembl
Innerchr15:46139544..46191159hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3851616
hg1951616
hg1851616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842495
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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