A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979816



Internal ID18615017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32505681..32510352hg38UCSC Ensembl
Innerchr3:32547173..32551844hg19UCSC Ensembl
Innerchr3:32522177..32526848hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg384672
hg194672
hg184672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2277345, nssv2277351, nssv2277343, nssv2277347, nssv2277344, nssv2277342, nssv2277348, nssv2277346, nssv2277350, nssv2277349
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)nsv979816
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