A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv266n21



Internal ID20131987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:199889..203266hg38UCSC Ensembl
chr3:241572..244949hg19UCSC Ensembl
chr3:216572..219949hg18UCSC Ensembl
chr3:216572..219949hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
hg173378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519754, nsv526215
Samples
Known GenesCHL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv266n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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