A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4340n100



Internal ID22790427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60986624..61017609hg38UCSC Ensembl
chr20:59561680..59592665hg19UCSC Ensembl
chr20:58995075..59026060hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3830986
hg1930986
hg1830986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056528, nsv1060818, nsv1064393, nsv1060520, nsv1059603, nsv1064669, nsv1062095, nsv1065195, nsv1056179, nsv1055955, nsv1060705, nsv1059686, nsv1062229, nsv1065688, nsv1060829, nsv1062317, nsv1060633, nsv1067244
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4340n100
Frequency
Sample Size11257
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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