A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694110



Internal ID15084076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10426592..10431934hg38UCSC Ensembl
Innerchr19:10537268..10542610hg19UCSC Ensembl
Innerchr19:10398268..10403610hg18UCSC Ensembl
Innerchr19:10398268..10403610hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385343
hg195343
hg185343
hg175343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521918
Supporting Variants
Samples
Known GenesPDE4A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694110
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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