A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968752



Internal ID18603980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125190068..125196501hg38UCSC Ensembl
Innerchr9:127952347..127958780hg19UCSC Ensembl
Innerchr9:126992168..126998601hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386434
hg196434
hg186434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2567244, nssv2566237, nssv2566242, nssv2566240, nssv2566238, nssv2566235, nssv2566241, nssv2566239, nssv2566243, nssv2566236
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)nsv968752
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