A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv281n21



Internal ID20132002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36387992..36415880hg38UCSC Ensembl
chr3:36429484..36457372hg19UCSC Ensembl
chr3:36404488..36432376hg18UCSC Ensembl
chr3:36404488..36432376hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3827889
hg1927889
hg1827889
hg1727889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518247, nsv523547
Samples
Known GenesSTAC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv281n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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