A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033995



Internal ID18776529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183357552..183463120hg38UCSC Ensembl
Innerchr4:184278705..184384273hg19UCSC Ensembl
Innerchr4:184515699..184621267hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38105569
hg19105569
hg18105569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635606
Samples
Known GenesCDKN2AIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033995
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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