A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv268n21



Internal ID20131989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:515117..1308774hg38UCSC Ensembl
chr3:556800..1350458hg19UCSC Ensembl
chr3:531800..1325458hg18UCSC Ensembl
chr3:531800..1325458hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38793658
hg19793659
hg18793659
hg17793659
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525119, nsv527054
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv268n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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