A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982415



Internal ID18617610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65164404..65169757hg38UCSC Ensembl
Innerchr9:42832350..42837723hg19UCSC Ensembl
Innerchr9:42822346..42827719hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385354
hg195374
hg185374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2732449, nssv2732451, nssv2732453, nssv2732450, nssv2732456, nssv2732457, nssv2732452, nssv2732455, nssv2732458, nssv2732454
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)nsv982415
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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