A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv85n82



Internal ID22782919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40254521..40258383hg38UCSC Ensembl
chr9:42399539..42403401hg19UCSC Ensembl
chr9:42389535..42393397hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383863
hg193863
hg183863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv973246, nsv982399
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)dgv85n82
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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