A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573528



Internal ID16360937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86695495..86722781hg38UCSC Ensembl
Innerchr16:86729101..86756387hg19UCSC Ensembl
Innerchr16:85286602..85313888hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3827287
hg1927287
hg1827287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862317
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573528
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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