A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978011



Internal ID18613216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88094046..88098229hg38UCSC Ensembl
Innerchr16:88127652..88131835hg19UCSC Ensembl
Innerchr16:86685153..86689336hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384184
hg194184
hg184184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2070029, nssv2070026, nssv2070034, nssv2070032, nssv2070031, nssv2070030, nssv2070033, nssv2070027, nssv2070035, nssv2070028
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)nsv978011
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