A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1946n100



Internal ID22788033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83390505..83477873hg38UCSC Ensembl
chr14:83856849..83944217hg19UCSC Ensembl
chr14:82926602..83013970hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3887369
hg1987369
hg1887369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054143, nsv1048281
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)dgv1946n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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