A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527267



Internal ID15107874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:713686..1101740hg38UCSC Ensembl
Innerchr3:755370..1143424hg19UCSC Ensembl
Innerchr3:730370..1118424hg18UCSC Ensembl
Innerchr3:730370..1118424hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38388055
hg19388055
hg18388055
hg17388055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703675
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527267
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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