A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982331



Internal ID18617526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101123174..101128665hg38UCSC Ensembl
Innerchr9:103885456..103890947hg19UCSC Ensembl
Innerchr9:102925277..102930768hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385492
hg195492
hg185492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563501, nssv2563502, nssv2563496, nssv2563500, nssv2563498, nssv2563497, nssv2563499, nssv2563495, nssv2563493, nssv2563494
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLPPR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982331
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