A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968643



Internal ID18603871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42831967..42974083hg38UCSC Ensembl
Innerchr9:43997036..44139152hg19UCSC Ensembl
Innerchr9:43937032..44079148hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38142117
hg19142117
hg18142117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2538888, nssv2538879, nssv2538881, nssv2538883, nssv2538887, nssv2538880, nssv2538885, nssv2538882, nssv2538884, nssv2538886
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)nsv968643
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer