A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978766



Internal ID18613969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8346486..8352560hg38UCSC Ensembl
Innerchr19:8411370..8417444hg19UCSC Ensembl
Innerchr19:8317370..8323444hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386075
hg196075
hg186075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2129422, nssv2129420, nssv2129428, nssv2129423, nssv2129424, nssv2129419, nssv2129426, nssv2129427, nssv2129421, nssv2129425
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)nsv978766
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