A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3376n100



Internal ID19013744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63137813..63195471hg38UCSC Ensembl
chr18:60805046..60862704hg19UCSC Ensembl
chr18:58956026..59013684hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3857659
hg1957659
hg1857659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059708, nsv1057080
Samples
Known GenesBCL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3376n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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