A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3301n100



Internal ID20154917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11543..326679hg38UCSC Ensembl
chr18:11543..326679hg19UCSC Ensembl
chr18:1543..316679hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38315137
hg19315137
hg18315137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061730, nsv1064673, nsv1059645
Samples
Known GenesCOLEC12, MIR8078, ROCK1P1, THOC1, USP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3301n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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