A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1879n100



Internal ID22787966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40476459..40575201hg38UCSC Ensembl
chr14:40945663..41044406hg19UCSC Ensembl
chr14:40015413..40114156hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3898743
hg1998744
hg1898744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036021, nsv1054904, nsv1043869
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)dgv1879n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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