A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3405n100



Internal ID22789492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76689670..76766320hg38UCSC Ensembl
chr18:74401627..74478276hg19UCSC Ensembl
chr18:72530615..72607264hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3876651
hg1976650
hg1876650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061460, nsv1056464, nsv1062458, nsv1058723, nsv1057424
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)dgv3405n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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