A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525745



Internal ID15453038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133001477..133039277hg38UCSC Ensembl
Innerchr12:133578063..133615863hg19UCSC Ensembl
Innerchr12:132088136..132125936hg18UCSC Ensembl
Innerchr12:132188413..132226213hg17UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3837801
hg1937801
hg1837801
hg1737801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701912
Samples
Known GenesZNF26, ZNF84
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525745
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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