A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521569



Internal ID15102176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1971892..2035996hg38UCSC Ensembl
Innerchr16:2021893..2085997hg19UCSC Ensembl
Innerchr16:1961894..2025998hg18UCSC Ensembl
Innerchr16:1961894..2025998hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3864105
hg1964105
hg1864105
hg1764105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698185
Samples
Known GenesGFER, NOXO1, NPW, SLC9A3R2, SYNGR3, TBL3, ZNF598
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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