A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573727



Internal ID16014450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89169527..89193067hg38UCSC Ensembl
Innerchr16:89235935..89259475hg19UCSC Ensembl
Innerchr16:87763436..87786976hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3823541
hg1923541
hg1823541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863309
Samples
Known GenesCDH15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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