A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3359n100



Internal ID22789446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56559549..56615362hg38UCSC Ensembl
chr18:54226780..54282593hg19UCSC Ensembl
chr18:52377778..52433591hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3855814
hg1955814
hg1855814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058023, nsv1057476
Samples
Known GenesTXNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3359n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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