A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv91n82



Internal ID22782925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62498723..62521809hg38UCSC Ensembl
chr9:46810024..46833110hg19UCSC Ensembl
chr9:46650020..46673106hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3823087
hg1923087
hg1823087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv973657, nsv972369
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC643648
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)dgv91n82
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer