A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv123n21



Internal ID20131844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21072704..21106531hg38UCSC Ensembl
chr14:21540863..21574690hg19UCSC Ensembl
chr14:20610703..20644530hg18UCSC Ensembl
chr14:20610703..20644530hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3833828
hg1933828
hg1833828
hg1733828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528337, nsv525724
Samples
Known GenesARHGEF40, TMEM253, ZNF219
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv123n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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