A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4292n100



Internal ID22790379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25851469..26324931hg38UCSC Ensembl
chr20:25832105..26305567hg19UCSC Ensembl
chr20:25780105..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38473463
hg19473463
hg18473463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059447, nsv1067411, nsv1060065, nsv1060508, nsv1057970, nsv1065198
Samples
Known GenesFAM182A, LOC100134868, LOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4292n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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