A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525234



Internal ID15105841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168843161..168848642hg38UCSC Ensembl
Innerchr4:169764312..169769793hg19UCSC Ensembl
Innerchr4:170000887..170006368hg18UCSC Ensembl
Innerchr4:170139042..170144523hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385482
hg195482
hg185482
hg175482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701323
Samples
Known GenesPALLD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525234
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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