A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3408n100



Internal ID22789495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78124860..78173537hg38UCSC Ensembl
chr18:75884860..75933537hg19UCSC Ensembl
chr18:73985848..74034525hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3848678
hg1948678
hg1848678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062257, nsv1059627, nsv1059070, nsv1063322
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)dgv3408n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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