A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4297n100



Internal ID20155913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30245152..30416523hg38UCSC Ensembl
chr20:29479828..29651199hg19UCSC Ensembl
chr20:28093489..28264860hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38171372
hg19171372
hg18171372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058387, nsv1067193
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4297n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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