A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1864n100



Internal ID22787951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33182514..33209026hg38UCSC Ensembl
chr14:33651720..33678232hg19UCSC Ensembl
chr14:32721471..32747983hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3826513
hg1926513
hg1826513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043765, nsv1042168, nsv1054895
Samples
Known GenesNPAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1864n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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