A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv29n21



Internal ID22766221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234468127..234477304hg38UCSC Ensembl
chr1:234603873..234613050hg19UCSC Ensembl
chr1:232670496..232679673hg18UCSC Ensembl
chr1:230910608..230919785hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg389178
hg199178
hg189178
hg179178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519695, nsv524608
Samples
Known GenesTARBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv29n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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