A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525548



Internal ID15106155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11169999..11272732hg38UCSC Ensembl
Innerchr16:11263856..11366589hg19UCSC Ensembl
Innerchr16:11171357..11274090hg18UCSC Ensembl
Innerchr16:11171357..11274090hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38102734
hg19102734
hg18102734
hg17102734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701686
Samples
Known GenesCLEC16A, SOCS1, TNP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525548
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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