A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3311n100



Internal ID22789398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1900056..1994942hg38UCSC Ensembl
chr18:1900057..1994943hg19UCSC Ensembl
chr18:1890057..1984943hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3894887
hg1994887
hg1894887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060293, nsv1066539, nsv1059347, nsv1064627, nsv1061326, nsv1064098, nsv1063610, nsv1063709, nsv1060583, nsv1066057, nsv1063124, nsv1057630, nsv1062043, nsv1055319, nsv1061135, nsv1057900, nsv1059831
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)dgv3311n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss149
Observed Complex0
Frequencyn/a


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