A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528251



Internal ID15108858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88398104..88488151hg38UCSC Ensembl
Innerchr16:88464512..88554559hg19UCSC Ensembl
Innerchr16:86992013..87082060hg18UCSC Ensembl
Innerchr16:86992013..87082060hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3890048
hg1990048
hg1890048
hg1790048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n21
Supporting Variantsnssv704817
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528251
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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