A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567135



Internal ID16354544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19795973..19812373hg38UCSC Ensembl
Innerchr15:20001226..20017626hg19UCSC Ensembl
Innerchr15:18261234..18277639hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3816401
hg1916401
hg1816406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv836866
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567135
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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