A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567136



Internal ID16354545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19795973..19850381hg38UCSC Ensembl
Innerchr15:20001226..20055634hg19UCSC Ensembl
Innerchr15:18261234..18315648hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3854409
hg1954409
hg1854415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv836867
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567136
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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