A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982211



Internal ID18617406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35449850..35451061hg38UCSC Ensembl
Innerchr9:35449847..35451058hg19UCSC Ensembl
Innerchr9:35439847..35441058hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381212
hg191212
hg181212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527734, nssv2527733, nssv2527730, nssv2527731, nssv2527728, nssv2527726, nssv2527732, nssv2527729, nssv2527725, nssv2527727
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesATP8B5P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982211
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