A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527054



Internal ID15107661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:515117..1308774hg38UCSC Ensembl
Innerchr3:556800..1350458hg19UCSC Ensembl
Innerchr3:531800..1325458hg18UCSC Ensembl
Innerchr3:531800..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 Variantsdgv268n21
Supporting Variantsnssv703430
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527054
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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