A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3703n54



Internal ID22771598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47116304..47198772hg38UCSC Ensembl
chr14:47585507..47667975hg19UCSC Ensembl
chr14:46655257..46737725hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3882469
hg1982469
hg1882469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564767, nsv564769, nsv564768, nsv564770
SamplesNINDS_178
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3703n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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