A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1880n100



Internal ID22787967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40737298..41068990hg38UCSC Ensembl
chr14:41206503..41538195hg19UCSC Ensembl
chr14:40276253..40607945hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38331693
hg19331693
hg18331693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047283, nsv1053355, nsv1054902
Samples
Known GenesLOC644919
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1880n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer