A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963384



Internal ID18598625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181864794..181867541hg38UCSC Ensembl
Innerchr3:181582582..181585329hg19UCSC Ensembl
Innerchr3:183065276..183068023hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg382748
hg192748
hg182748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2306530, nssv2306527, nssv2306535, nssv2306531, nssv2306534, nssv2306533, nssv2306529, nssv2306526, nssv2306532, nssv2306528
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)nsv963384
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