A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982317



Internal ID18617512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87855517..87861341hg38UCSC Ensembl
Innerchr9:90470432..90476256hg19UCSC Ensembl
Innerchr9:89660252..89666076hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385825
hg195825
hg185825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2557763, nssv2557760, nssv2557756, nssv2557758, nssv2557757, nssv2557759, nssv2557762, nssv2557754, nssv2557761, nssv2557755
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC392364
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982317
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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