A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528456



Internal ID15109063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88321646..88485962hg38UCSC Ensembl
Innerchr16:88355252..88552370hg19UCSC Ensembl
Innerchr16:86912753..87079871hg18UCSC Ensembl
Innerchr16:86912753..87079871hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38164317
hg19197119
hg18167119
hg17167119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705058
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528456
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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