A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1806n100



Internal ID22787893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22130412..22509792hg38UCSC Ensembl
chr14:22598376..22978775hg19UCSC Ensembl
chr14:21668216..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38379381
hg19380400
hg18380400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041100, nsv1041751, nsv1040360, nsv1043480, nsv1047956, nsv1049940, nsv1038500, nsv1037374, nsv1040078
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)dgv1806n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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