A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1980n100



Internal ID22788067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104494679..104570679hg38UCSC Ensembl
chr14:104961016..105037016hg19UCSC Ensembl
chr14:104032061..104108061hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3876001
hg1976001
hg1876001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054482, nsv1035993
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)dgv1980n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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