A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1921n100



Internal ID22788008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55926860..55961442hg38UCSC Ensembl
chr14:56393578..56428160hg19UCSC Ensembl
chr14:55463331..55497913hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3834583
hg1934583
hg1834583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040791, nsv1043948, nsv1048063
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1921n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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