A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1932n100



Internal ID22788019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73237039..73268468hg38UCSC Ensembl
chr14:73703747..73735176hg19UCSC Ensembl
chr14:72773500..72804929hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3831430
hg1931430
hg1831430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051573, nsv1051216
Samples
Known GenesPAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1932n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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