A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525119



Internal ID15105726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:524278..1296575hg38UCSC Ensembl
Innerchr3:565961..1338259hg19UCSC Ensembl
Innerchr3:540961..1313259hg18UCSC Ensembl
Innerchr3:540961..1313259hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38772298
hg19772299
hg18772299
hg17772299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n21
Supporting Variantsnssv701184
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525119
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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