A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1905n100



Internal ID22787992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45284734..45555776hg38UCSC Ensembl
chr14:45753937..46024979hg19UCSC Ensembl
chr14:44823687..45094729hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38271043
hg19271043
hg18271043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040279, nsv1040813, nsv1052588, nsv1043014, nsv1048492, nsv1042444, nsv1039520
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)dgv1905n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss79
Observed Complex0
Frequencyn/a


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