A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525966



Internal ID15106573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11667074..12124663hg38UCSC Ensembl
Innerchr19:11777889..12235478hg19UCSC Ensembl
Innerchr19:11638889..12096478hg18UCSC Ensembl
Innerchr19:11638889..12096478hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38457590
hg19457590
hg18457590
hg17457590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702180
Samples
Known GenesZNF433, ZNF439, ZNF440, ZNF441, ZNF491, ZNF69, ZNF700, ZNF763, ZNF788, ZNF823, ZNF833P, ZNF844, ZNF878
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525966
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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