A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968754



Internal ID18603982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138231177..138257640hg38UCSC Ensembl
Innerchr9:141121627..141148090hg19UCSC Ensembl
Innerchr9:140241448..140267911hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3826464
hg1926464
hg1826464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2569965, nssv2569963, nssv2569960, nssv2569968, nssv2569967, nssv2569964, nssv2569961, nssv2569962, nssv2569966, nssv2569959
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM157B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968754
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