A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1888n100



Internal ID22787975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42489030..42655964hg38UCSC Ensembl
chr14:42958233..43125167hg19UCSC Ensembl
chr14:42027983..42194917hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38166935
hg19166935
hg18166935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042451, nsv1041777, nsv1049568, nsv1042236
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)dgv1888n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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