A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982316



Internal ID18617511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87817074..87818550hg38UCSC Ensembl
Innerchr9:90431989..90433465hg19UCSC Ensembl
Innerchr9:89621809..89623285hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381477
hg191477
hg181477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557569, nssv2557567, nssv2557565, nssv2557563, nssv2557564, nssv2557561, nssv2557562, nssv2557568, nssv2557566, nssv2557560
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982316
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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