A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982291



Internal ID18617486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63975361..63977698hg38UCSC Ensembl
Innerchr9:69219108..69221118hg19UCSC Ensembl
Innerchr9:68508928..68510938hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382338
hg192011
hg182011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2550555, nssv2550553, nssv2550554, nssv2550550, nssv2550551, nssv2550548, nssv2550552, nssv2550549, nssv2550546, nssv2550547
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982291
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