A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4296n100



Internal ID22790383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30185664..30400778hg38UCSC Ensembl
chr20:29420340..29635454hg19UCSC Ensembl
chr20:28034001..28249115hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38215115
hg19215115
hg18215115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062766, nsv1059061
Samples
Known GenesFRG1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4296n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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