A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv89n82



Internal ID22782923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42547832..42579451hg38UCSC Ensembl
chr9:44391520..44423328hg19UCSC Ensembl
chr9:44331516..44363324hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3831620
hg1931809
hg1831809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv982254, nsv972354
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)dgv89n82
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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