A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1795n100



Internal ID22787882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19924443..19956767hg38UCSC Ensembl
chr14:20392602..20424926hg19UCSC Ensembl
chr14:19462442..19494766hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3832325
hg1932325
hg1832325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042373, nsv1044821
Samples
Known GenesOR4K1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1795n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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