A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3389n100



Internal ID22789476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67941356..68116392hg38UCSC Ensembl
chr18:65608593..65783629hg19UCSC Ensembl
chr18:63759573..63934609hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38175037
hg19175037
hg18175037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060561, nsv1057907, nsv1063821
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)dgv3389n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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