A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv139n21



Internal ID22766331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81670496..81707997hg38UCSC Ensembl
chr14:82136840..82174341hg19UCSC Ensembl
chr14:81206593..81244094hg18UCSC Ensembl
chr14:81206593..81244094hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3837502
hg1937502
hg1837502
hg1737502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523456, nsv521291
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv139n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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