A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4833n100



Internal ID22790920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105835736..105926526hg38UCSC Ensembl
chr3:105554580..105645373hg19UCSC Ensembl
chr3:107037270..107128063hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3890791
hg1990794
hg1890794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008876, nsv1008564
Samples
Known GenesCBLB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4833n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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