A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1801n100



Internal ID20153417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20880514..20934425hg38UCSC Ensembl
chr14:21348673..21402584hg19UCSC Ensembl
chr14:20418513..20472424hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3853912
hg1953912
hg1853912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040201, nsv1040447
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1801n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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