A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3364n100



Internal ID20154980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58350291..58452397hg38UCSC Ensembl
chr18:56017523..56119629hg19UCSC Ensembl
chr18:54168503..54270609hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38102107
hg19102107
hg18102107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062938, nsv1058838, nsv1067389, nsv1055652, nsv1065132
Samples
Known GenesMIR122, MIR3591, NEDD4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3364n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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