A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965145



Internal ID18600379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15373395..15376120hg38UCSC Ensembl
Innerchr3:15414902..15417627hg19UCSC Ensembl
Innerchr3:15389906..15392631hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382726
hg192726
hg182726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274712, nssv2274721, nssv2274719, nssv2274720, nssv2274714, nssv2274717, nssv2274713, nssv2274715, nssv2274716, nssv2274718
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)nsv965145
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