A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1968n100



Internal ID22788055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98707831..98731044hg38UCSC Ensembl
chr14:99174168..99197381hg19UCSC Ensembl
chr14:98243921..98267134hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3823214
hg1923214
hg1823214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048088, nsv1035747
Samples
Known GenesC14orf177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1968n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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