A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982241



Internal ID18617436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39877863..40101911hg38UCSC Ensembl
Innerchr9:42022881..42246929hg19UCSC Ensembl
Innerchr9:42012881..42236925hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38224049
hg19224049
hg18224045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2535817, nssv2535816, nssv2535812, nssv2535815, nssv2535814, nssv2535813, nssv2535810, nssv2535819, nssv2535811, nssv2535818
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)nsv982241
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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