A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960658



Internal ID18595905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14362872..14430234hg38UCSC Ensembl
Innerchr18:14362871..14430233hg19UCSC Ensembl
Innerchr18:14352871..14420233hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3867363
hg1967363
hg1867363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2117216, nssv2117210, nssv2117218, nssv2117211, nssv2117217, nssv2117214, nssv2117213, nssv2117219, nssv2117215, nssv2117212
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)nsv960658
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