A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv92n82



Internal ID22782926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67913212..67919820hg38UCSC Ensembl
chr9:67980658..67987266hg19UCSC Ensembl
chr9:67570478..67577086hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386609
hg196609
hg186609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv982498, nsv969660
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)dgv92n82
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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