A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv332n21



Internal ID20132053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187966266..188141060hg38UCSC Ensembl
chr4:188887420..189062214hg19UCSC Ensembl
chr4:189124414..189299208hg18UCSC Ensembl
chr4:189262569..189437363hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38174795
hg19174795
hg18174795
hg17174795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518420, nsv522793
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv332n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer