A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569335



Internal ID16356744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47814724..48058126hg38UCSC Ensembl
Innerchr15:48106921..48350323hg19UCSC Ensembl
Innerchr15:45894213..46137615hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38243403
hg19243403
hg18243403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149597
SamplesHGDP00741
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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